Canonical Allele Identifier: CA467779961

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136130684G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255297G>A , CM000671.2:g.133255297G>A	GRCh38
NC_000009.11:g.136130684G>A , CM000671.1:g.136130684G>A	GRCh37
NC_000009.10:g.135120505G>A	NCBI36
NG_006669.1:g.22371C>T
NG_006669.2:g.24919C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.1463C>T
ENST00000647353.1:n.54-4145C>T
ENST00000679909.1:c.28+19865C>T	ENSP00000506089.1:n.28+19865C>T
ENST00000453660.3:n.1445C>T
ENST00000611156.4:c.*369C>T	ENSP00000483265.1:n.*369C>T
NM_020469.2:c.*369C>T	NP_065202.2:n.*369C>T
NM_020469.3:c.*369C>T	NP_065202.2:n.*369C>T