Canonical Allele Identifier: CA467780095

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136130722T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255335T>A , CM000671.2:g.133255335T>A	GRCh38
NC_000009.11:g.136130722T>A , CM000671.1:g.136130722T>A	GRCh37
NC_000009.10:g.135120543T>A	NCBI36
NG_006669.1:g.22333A>T
NG_006669.2:g.24881A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.1425A>T
ENST00000647353.1:n.54-4183A>T
ENST00000679909.1:c.28+19827A>T	ENSP00000506089.1:n.28+19827A>T
ENST00000453660.3:n.1407A>T
ENST00000611156.4:c.*331A>T	ENSP00000483265.1:n.*331A>T
NM_020469.2:c.*331A>T	NP_065202.2:n.*331A>T
NM_020469.3:c.*331A>T	NP_065202.2:n.*331A>T