Canonical Allele Identifier: CA437358383

Gene: AHSG

Linked Data

• gnomAD v4: 3-186620648-C-T
• MyVariant Identifiers: chr3:g.186338437C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186620648C>T , CM000665.2:g.186620648C>T	GRCh38
NC_000003.11:g.186338437C>T , CM000665.1:g.186338437C>T	GRCh37
NC_000003.10:g.187821131C>T	NCBI36
NG_011436.1:g.12588C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411641.7:c.822C>T MANE Select	ENSP00000393887.2:p.Asp274=
ENST00000273784.5:c.825C>T	ENSP00000273784.5:p.Asp275=
ENST00000411641.6:c.822C>T	ENSP00000393887.2:p.Asp274=
NM_001622.2:c.822C>T	NP_001613.2:p.Asp274=
NM_001354571.1:c.825C>T	NP_001341500.1:p.Asp275=
NM_001354572.1:c.819C>T	NP_001341501.1:p.Asp273=
NM_001354573.1:c.738C>T	NP_001341502.1:p.Asp246=
NM_001622.3:c.822C>T	NP_001613.2:p.Asp274=
NM_001622.4:c.822C>T MANE Select	NP_001613.2:p.Asp274=
NM_001354571.2:c.825C>T	NP_001341500.1:p.Asp275=
NM_001354572.2:c.819C>T	NP_001341501.1:p.Asp273=
NM_001354573.2:c.738C>T	NP_001341502.1:p.Asp246=