Canonical Allele Identifier: CA437358375
Gene: AHSG HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.186338434G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186620645G>T , CM000665.2:g.186620645G>T GRCh38
NC_000003.11:g.186338434G>T , CM000665.1:g.186338434G>T GRCh37
NC_000003.10:g.187821128G>T NCBI36
NG_011436.1:g.12585G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000411641.7:c.819G>T MANE Select ENSP00000393887.2:p.Val273=
ENST00000273784.5:c.822G>T ENSP00000273784.5:p.Val274=
ENST00000411641.6:c.819G>T ENSP00000393887.2:p.Val273=
NM_001622.2:c.819G>T NP_001613.2:p.Val273=
NM_001354571.1:c.822G>T NP_001341500.1:p.Val274=
NM_001354572.1:c.816G>T NP_001341501.1:p.Val272=
NM_001354573.1:c.735G>T NP_001341502.1:p.Val245=
NM_001622.3:c.819G>T NP_001613.2:p.Val273=
NM_001622.4:c.819G>T MANE Select NP_001613.2:p.Val273=
NM_001354571.2:c.822G>T NP_001341500.1:p.Val274=
NM_001354572.2:c.816G>T NP_001341501.1:p.Val272=
NM_001354573.2:c.735G>T NP_001341502.1:p.Val245=