Canonical Allele Identifier: CA375686198

Gene: ABO

Linked Data

• gnomAD v4: 9-133256209-C-A
• MyVariant Identifiers: chr9:g.136131596C>A (hg19) ; chr9:g.133256209C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256209C>A , CM000671.2:g.133256209C>A	GRCh38
NC_000009.11:g.136131596C>A , CM000671.1:g.136131596C>A	GRCh37
NC_000009.10:g.135121417C>A	NCBI36
NG_006669.1:g.21459G>T
NG_006669.2:g.24007G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.551G>T
ENST00000647353.1:n.54-5057G>T
ENST00000651471.1:n.477G>T
ENST00000679909.1:c.28+18953G>T	ENSP00000506089.1:n.28+18953G>T
ENST00000453660.3:n.533G>T
ENST00000538324.2:c.519G>T	ENSP00000483018.1:p.Glu173Asp
ENST00000611156.4:c.519G>T	ENSP00000483265.1:p.Glu173Asp
NM_020469.2:c.522G>T	NP_065202.2:p.Glu174Asp
NM_020469.3:c.522G>T	NP_065202.2:p.Glu174Asp