Linked Data
dbSNP Id:
rs766105817
ExAC:
17:42030489 G / T
gnomAD v2:
17-42030489-G-T
gnomAD v3:
17-43953121-G-T
gnomAD v4:
17-43953121-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.43953121G>T , CM000679.2:g.43953121G>T | GRCh38 |
| NC_000017.10:g.42030489G>T , CM000679.1:g.42030489G>T | GRCh37 |
| NC_000017.9:g.39386015G>T | NCBI36 |
| NG_023338.1:g.56349C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000592796.2:c.257C>A | ENSP00000467310.1:p.Pro86His | |
| ENST00000692052.1:c.257C>A MANE Select | ENSP00000509262.1:p.Pro86His | |
| ENST00000360085.6:c.257C>A | ENSP00000353198.1:p.Pro86His | |
| ENST00000592796.1:c.257C>A | ENSP00000467310.1:p.Pro86His | |
| NM_004160.4:c.257C>A | NP_004151.3:p.Pro86His | |
| XM_011525035.1:c.257C>A | XP_011523337.1:p.Pro86His | |
| NM_004160.5:c.257C>A | NP_004151.3:p.Pro86His | |
| NM_001394028.1:c.257C>A MANE Select | NP_001380957.1:p.Pro86His | |
| NM_001394029.1:c.257C>A | NP_001380958.1:p.Pro86His | |
| NM_004160.6:c.257C>A | NP_004151.4:p.Pro86His |