Linked Data
ClinVar Variation Id:
509992
ClinVar RCV Id:
RCV000601763
dbSNP Id:
rs1483246379
gnomAD v2:
X-18525199-A-G
gnomAD v4:
X-18507079-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.18507079A>G , CM000685.2:g.18507079A>G | GRCh38 |
| NC_000023.10:g.18525199A>G , CM000685.1:g.18525199A>G | GRCh37 |
| NC_000023.9:g.18435120A>G | NCBI36 |
| NG_008475.1:g.86475A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000623535.2:c.-18A>G MANE Select | ENSP00000485244.1:n.-18A>G | |
| ENST00000635828.1:c.-18A>G | ENSP00000490170.1:n.-18A>G | |
| ENST00000637881.1:c.-18A>G | ENSP00000489879.1:n.-18A>G | |
| ENST00000674046.1:c.-18A>G | ENSP00000501174.1:n.-18A>G | |
| ENST00000379989.6:c.-18A>G | ENSP00000369325.3:n.-18A>G | |
| ENST00000379996.7:c.-18A>G | ENSP00000369332.3:n.-18A>G | |
| ENST00000463994.4:c.-18A>G | ENSP00000485184.1:n.-18A>G | |
| ENST00000623364.3:c.-18A>G | ENSP00000485581.1:n.-18A>G | |
| ENST00000624700.3:c.-18A>G | ENSP00000485359.1:n.-18A>G | |
| ENST00000624953.1:c.-18A>G | ENSP00000485625.1:n.-18A>G | |
| NM_001037343.1:c.-18A>G | NP_001032420.1:n.-18A>G | |
| NM_003159.2:c.-18A>G | NP_003150.1:n.-18A>G | |
| XM_011545569.1:c.-18A>G | XP_011543871.1:n.-18A>G | |
| XM_011545570.1:c.-104A>G | XP_011543872.1:n.-104A>G | |
| XR_950484.1:n.235A>G | ||
| NM_001323289.1:c.-18A>G | NP_001310218.1:n.-18A>G | |
| NM_001323289.2:c.-18A>G MANE Select | NP_001310218.1:n.-18A>G | |
| NM_001037343.2:c.-18A>G | NP_001032420.1:n.-18A>G | |
| NM_003159.3:c.-18A>G | NP_003150.1:n.-18A>G |