Canonical Allele Identifier: CA375686187

Gene: ABO

Linked Data

• gnomAD v4: 9-133256201-G-T
• MyVariant Identifiers: chr9:g.136131588G>T (hg19) ; chr9:g.133256201G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256201G>T , CM000671.2:g.133256201G>T	GRCh38
NC_000009.11:g.136131588G>T , CM000671.1:g.136131588G>T	GRCh37
NC_000009.10:g.135121409G>T	NCBI36
NG_006669.1:g.21467C>A
NG_006669.2:g.24015C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.559C>A
ENST00000647353.1:n.54-5049C>A
ENST00000651471.1:n.485C>A
ENST00000679909.1:c.28+18961C>A	ENSP00000506089.1:n.28+18961C>A
ENST00000453660.3:n.541C>A
ENST00000538324.2:c.527C>A	ENSP00000483018.1:p.Ala176Asp
ENST00000611156.4:c.527C>A	ENSP00000483265.1:p.Ala176Asp
NM_020469.2:c.530C>A	NP_065202.2:p.Ala177Asp
NM_020469.3:c.530C>A	NP_065202.2:p.Ala177Asp