ClinVar Variation:
dbSNP:
gnomAD v2:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.63941854C>T , CM000679.2:g.63941854C>T | GRCh38 |
| NC_000017.10:g.62019214C>T , CM000679.1:g.62019214C>T | GRCh37 |
| NC_000017.9:g.59372946C>T | NCBI36 |
| NG_011699.1:g.36065G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000435607.3:c.4428G>A MANE Select | ENSP00000396320.1:p.Met1476Ile | |
| ENST00000578147.5:c.4428G>A | ENSP00000463963.1:p.Met1476Ile | |
| NM_000334.4:c.4428G>A MANE Select | NP_000325.4:p.Met1476Ile | |
| XM_005257566.3:c.4428G>A | XP_005257623.1:p.Met1476Ile |