Linked Data
ClinVar Variation Id:
102647
dbSNP Id:
rs62508575
gnomAD v3:
12-102917129-A-C
gnomAD v4:
12-102917129-A-C
ERepo:
CA229509/MONDO:0009861/006
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.102917129A>C , CM000674.2:g.102917129A>C | GRCh38 |
| NC_000012.11:g.103310907A>C , CM000674.1:g.103310907A>C | GRCh37 |
| NC_000012.10:g.101835037A>C | NCBI36 |
| NG_008690.1:g.5474T>G | |
| NG_008690.2:g.46282T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000553106.6:c.2T>G MANE Select | ENSP00000448059.1:p.Met1Arg | |
| ENST00000307000.7:c.-146T>G | ENSP00000303500.2:n.-146T>G | |
| ENST00000546844.1:c.2T>G | ENSP00000446658.1:p.Met1Arg | |
| ENST00000547319.1:n.313T>G | ||
| ENST00000549111.5:n.98T>G | ||
| ENST00000551337.5:c.2T>G | ENSP00000447620.1:p.Met1Arg | |
| ENST00000551988.5:n.91T>G | ||
| ENST00000553106.5:c.2T>G | ENSP00000448059.1:p.Met1Arg | |
| ENST00000635500.1:n.29-4231T>G | ||
| NM_000277.1:c.2T>G | NP_000268.1:p.Met1Arg | |
| XM_011538422.1:c.2T>G | XP_011536724.1:p.Met1Arg | |
| NM_000277.2:c.2T>G | NP_000268.1:p.Met1Arg | |
| NM_001354304.1:c.2T>G | NP_001341233.1:p.Met1Arg | |
| XM_017019370.2:c.2T>G | XP_016874859.1:p.Met1Arg | |
| NM_000277.3:c.2T>G MANE Select | NP_000268.1:p.Met1Arg | |
| NM_001354304.2:c.2T>G | NP_001341233.1:p.Met1Arg |