Canonical Allele Identifier: CA437358387

Gene: AHSG

Linked Data

• MyVariant Identifiers: chr3:g.186338440A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186620651A>C , CM000665.2:g.186620651A>C	GRCh38
NC_000003.11:g.186338440A>C , CM000665.1:g.186338440A>C	GRCh37
NC_000003.10:g.187821134A>C	NCBI36
NG_011436.1:g.12591A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000411641.7:c.825A>C MANE Select	ENSP00000393887.2:p.Pro275=
ENST00000273784.5:c.828A>C	ENSP00000273784.5:p.Pro276=
ENST00000411641.6:c.825A>C	ENSP00000393887.2:p.Pro275=
NM_001622.2:c.825A>C	NP_001613.2:p.Pro275=
NM_001354571.1:c.828A>C	NP_001341500.1:p.Pro276=
NM_001354572.1:c.822A>C	NP_001341501.1:p.Pro274=
NM_001354573.1:c.741A>C	NP_001341502.1:p.Pro247=
NM_001622.3:c.825A>C	NP_001613.2:p.Pro275=
NM_001622.4:c.825A>C MANE Select	NP_001613.2:p.Pro275=
NM_001354571.2:c.828A>C	NP_001341500.1:p.Pro276=
NM_001354572.2:c.822A>C	NP_001341501.1:p.Pro274=
NM_001354573.2:c.741A>C	NP_001341502.1:p.Pro247=