Canonical Allele Identifier: CA467782884

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136131602C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256215C>T , CM000671.2:g.133256215C>T	GRCh38
NC_000009.11:g.136131602C>T , CM000671.1:g.136131602C>T	GRCh37
NC_000009.10:g.135121423C>T	NCBI36
NG_006669.1:g.21453G>A
NG_006669.2:g.24001G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.545G>A
ENST00000647353.1:n.54-5063G>A
ENST00000651471.1:n.471G>A
ENST00000679909.1:c.28+18947G>A	ENSP00000506089.1:n.28+18947G>A
ENST00000453660.3:n.527G>A
ENST00000538324.2:c.513G>A	ENSP00000483018.1:p.Val171=
ENST00000611156.4:c.513G>A	ENSP00000483265.1:p.Val171=
NM_020469.2:c.516G>A	NP_065202.2:p.Val172=
NM_020469.3:c.516G>A	NP_065202.2:p.Val172=