Canonical Allele Identifier: CA2668958131

Gene: AHSG

Linked Data

• gnomAD v4: 3-186617856-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186617856G>C , CM000665.2:g.186617856G>C	GRCh38
NC_000003.11:g.186335645G>C , CM000665.1:g.186335645G>C	GRCh37
NC_000003.10:g.187818339G>C	NCBI36
NG_011436.1:g.9796G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411641.7:c.573+506G>C MANE Select	ENSP00000393887.2:n.573+506G>C
ENST00000273784.5:c.576+506G>C	ENSP00000273784.5:n.576+506G>C
ENST00000411641.6:c.573+506G>C	ENSP00000393887.2:n.573+506G>C
ENST00000478441.1:n.1136G>C
NM_001622.2:c.573+506G>C	NP_001613.2:n.573+506G>C
NM_001354571.1:c.576+506G>C	NP_001341500.1:n.576+506G>C
NM_001354572.1:c.570+506G>C	NP_001341501.1:n.570+506G>C
NM_001354573.1:c.573+506G>C	NP_001341502.1:n.573+506G>C
NM_001622.3:c.573+506G>C	NP_001613.2:n.573+506G>C
NM_001622.4:c.573+506G>C MANE Select	NP_001613.2:n.573+506G>C
NM_001354571.2:c.576+506G>C	NP_001341500.1:n.576+506G>C
NM_001354572.2:c.570+506G>C	NP_001341501.1:n.570+506G>C
NM_001354573.2:c.573+506G>C	NP_001341502.1:n.573+506G>C