Canonical Allele Identifier: CA467782913

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136131638G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256251G>T , CM000671.2:g.133256251G>T	GRCh38
NC_000009.11:g.136131638G>T , CM000671.1:g.136131638G>T	GRCh37
NC_000009.10:g.135121459G>T	NCBI36
NG_006669.1:g.21417C>A
NG_006669.2:g.23965C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.509C>A
ENST00000647353.1:n.54-5099C>A
ENST00000651471.1:n.435C>A
ENST00000679909.1:c.28+18911C>A	ENSP00000506089.1:n.28+18911C>A
ENST00000453660.3:n.491C>A
ENST00000538324.2:c.477C>A	ENSP00000483018.1:p.Pro159=
ENST00000611156.4:c.477C>A	ENSP00000483265.1:p.Pro159=
NM_020469.2:c.480C>A	NP_065202.2:p.Pro160=
NM_020469.3:c.480C>A	NP_065202.2:p.Pro160=