Canonical Allele Identifier: CA467780078

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136130717G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255330G>A , CM000671.2:g.133255330G>A	GRCh38
NC_000009.11:g.136130717G>A , CM000671.1:g.136130717G>A	GRCh37
NC_000009.10:g.135120538G>A	NCBI36
NG_006669.1:g.22338C>T
NG_006669.2:g.24886C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.1430C>T
ENST00000647353.1:n.54-4178C>T
ENST00000679909.1:c.28+19832C>T	ENSP00000506089.1:n.28+19832C>T
ENST00000453660.3:n.1412C>T
ENST00000611156.4:c.*336C>T	ENSP00000483265.1:n.*336C>T
NM_020469.2:c.*336C>T	NP_065202.2:n.*336C>T
NM_020469.3:c.*336C>T	NP_065202.2:n.*336C>T