Linked Data
ClinVar Variation Id:
1703224
ClinVar RCV Id:
RCV002280347
MyVariant Identifiers:
chr1:g.171621380C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.171652240C>G , CM000663.2:g.171652240C>G | GRCh38 |
| NC_000001.10:g.171621380C>G , CM000663.1:g.171621380C>G | GRCh37 |
| NC_000001.9:g.169888003C>G | NCBI36 |
| NG_008859.1:g.5394G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000037502.11:c.372G>C MANE Select | ENSP00000037502.5:p.Leu124= | |
| ENST00000638471.1:c.130+242G>C | ENSP00000491206.1:n.130+242G>C | |
| ENST00000037502.10:c.372G>C | ENSP00000037502.5:p.Leu124= | |
| ENST00000614688.1:c.372G>C | ENSP00000478680.1:p.Leu124= | |
| NM_000261.1:c.372G>C | NP_000252.1:p.Leu124= | |
| NM_000261.2:c.372G>C MANE Select | NP_000252.1:p.Leu124= |