Canonical Allele Identifier: CA355714434

Gene: AHSG

Linked Data

• MyVariant Identifiers: chr3:g.186336329T>C (hg19) ; chr3:g.186618540T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186618540T>C , CM000665.2:g.186618540T>C	GRCh38
NC_000003.11:g.186336329T>C , CM000665.1:g.186336329T>C	GRCh37
NC_000003.10:g.187819023T>C	NCBI36
NG_011436.1:g.10480T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411641.7:c.578T>C MANE Select	ENSP00000393887.2:p.Leu193Pro
ENST00000273784.5:c.581T>C	ENSP00000273784.5:p.Leu194Pro
ENST00000411641.6:c.578T>C	ENSP00000393887.2:p.Leu193Pro
NM_001622.2:c.578T>C	NP_001613.2:p.Leu193Pro
NM_001354571.1:c.581T>C	NP_001341500.1:p.Leu194Pro
NM_001354572.1:c.575T>C	NP_001341501.1:p.Leu192Pro
NM_001354573.1:c.578T>C	NP_001341502.1:p.Leu193Pro
NM_001622.3:c.578T>C	NP_001613.2:p.Leu193Pro
NM_001622.4:c.578T>C MANE Select	NP_001613.2:p.Leu193Pro
NM_001354571.2:c.581T>C	NP_001341500.1:p.Leu194Pro
NM_001354572.2:c.575T>C	NP_001341501.1:p.Leu192Pro
NM_001354573.2:c.578T>C	NP_001341502.1:p.Leu193Pro