Canonical Allele Identifier: CA375683590

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136131122C>A (hg19) ; chr9:g.133255735C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255735C>A , CM000671.2:g.133255735C>A	GRCh38
NC_000009.11:g.136131122C>A , CM000671.1:g.136131122C>A	GRCh37
NC_000009.10:g.135120943C>A	NCBI36
NG_006669.1:g.21933G>T
NG_006669.2:g.24481G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.1025G>T
ENST00000647353.1:n.54-4583G>T
ENST00000679909.1:c.28+19427G>T	ENSP00000506089.1:n.28+19427G>T
ENST00000453660.3:n.1007G>T
ENST00000538324.2:c.993G>T	ENSP00000483018.1:p.Trp331Cys
ENST00000611156.4:c.993G>T	ENSP00000483265.1:p.Trp331Cys
NM_020469.2:c.996G>T	NP_065202.2:p.Trp332Cys
NM_020469.3:c.996G>T	NP_065202.2:p.Trp332Cys