Linked Data
ClinVar Variation Id:
2982653
ClinVar RCV Id:
RCV003845284
dbSNP Id:
rs752460880
ExAC:
12:103271230 A / G
gnomAD v2:
12-103271230-A-G
gnomAD v4:
12-102877452-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.102877452A>G , CM000674.2:g.102877452A>G | GRCh38 |
| NC_000012.11:g.103271230A>G , CM000674.1:g.103271230A>G | GRCh37 |
| NC_000012.10:g.101795360A>G | NCBI36 |
| NG_008690.1:g.45151T>C | |
| NG_008690.2:g.85959T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000553106.6:c.441+10T>C MANE Select | ENSP00000448059.1:n.441+10T>C | |
| ENST00000307000.7:c.426+10T>C | ENSP00000303500.2:n.426+10T>C | |
| ENST00000549111.5:n.537+10T>C | ||
| ENST00000550978.6:c.435T>C | ||
| ENST00000551988.5:n.530+10T>C | ||
| ENST00000553106.5:c.441+10T>C | ENSP00000448059.1:n.441+10T>C | |
| NM_000277.1:c.441+10T>C | NP_000268.1:n.441+10T>C | |
| XM_011538422.1:c.441+10T>C | XP_011536724.1:n.441+10T>C | |
| NM_000277.2:c.441+10T>C | NP_000268.1:n.441+10T>C | |
| NM_001354304.1:c.441+10T>C | NP_001341233.1:n.441+10T>C | |
| XM_017019370.2:c.441+10T>C | XP_016874859.1:n.441+10T>C | |
| NM_000277.3:c.441+10T>C MANE Select | NP_000268.1:n.441+10T>C | |
| NM_001354304.2:c.441+10T>C | NP_001341233.1:n.441+10T>C |