Canonical Allele Identifier: CA1427018388

Gene: AHSG

Linked Data

• dbSNP Id: rs1716357328
• gnomAD v4: 3-186617859-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186617859T>C , CM000665.2:g.186617859T>C	GRCh38
NC_000003.11:g.186335648T>C , CM000665.1:g.186335648T>C	GRCh37
NC_000003.10:g.187818342T>C	NCBI36
NG_011436.1:g.9799T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411641.7:c.573+509T>C MANE Select	ENSP00000393887.2:n.573+509T>C
ENST00000273784.5:c.576+509T>C	ENSP00000273784.5:n.576+509T>C
ENST00000411641.6:c.573+509T>C	ENSP00000393887.2:n.573+509T>C
ENST00000478441.1:n.1139T>C
NM_001622.2:c.573+509T>C	NP_001613.2:n.573+509T>C
NM_001354571.1:c.576+509T>C	NP_001341500.1:n.576+509T>C
NM_001354572.1:c.570+509T>C	NP_001341501.1:n.570+509T>C
NM_001354573.1:c.573+509T>C	NP_001341502.1:n.573+509T>C
NM_001622.3:c.573+509T>C	NP_001613.2:n.573+509T>C
NM_001622.4:c.573+509T>C MANE Select	NP_001613.2:n.573+509T>C
NM_001354571.2:c.576+509T>C	NP_001341500.1:n.576+509T>C
NM_001354572.2:c.570+509T>C	NP_001341501.1:n.570+509T>C
NM_001354573.2:c.573+509T>C	NP_001341502.1:n.573+509T>C