Canonical Allele Identifier: CA375686163

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136131577A>T (hg19) ; chr9:g.133256190A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256190A>T , CM000671.2:g.133256190A>T	GRCh38
NC_000009.11:g.136131577A>T , CM000671.1:g.136131577A>T	GRCh37
NC_000009.10:g.135121398A>T	NCBI36
NG_006669.1:g.21478T>A
NG_006669.2:g.24026T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.570T>A
ENST00000647353.1:n.54-5038T>A
ENST00000651471.1:n.496T>A
ENST00000679909.1:c.28+18972T>A	ENSP00000506089.1:n.28+18972T>A
ENST00000453660.3:n.552T>A
ENST00000538324.2:c.538T>A	ENSP00000483018.1:p.Trp180Arg
ENST00000611156.4:c.538T>A	ENSP00000483265.1:p.Trp180Arg
NM_020469.2:c.541T>A	NP_065202.2:p.Trp181Arg
NM_020469.3:c.541T>A	NP_065202.2:p.Trp181Arg