Canonical Allele Identifier: CA467781361

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136130911G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255524G>A , CM000671.2:g.133255524G>A	GRCh38
NC_000009.11:g.136130911G>A , CM000671.1:g.136130911G>A	GRCh37
NC_000009.10:g.135120732G>A	NCBI36
NG_006669.1:g.22144C>T
NG_006669.2:g.24692C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.1236C>T
ENST00000647353.1:n.54-4372C>T
ENST00000679909.1:c.28+19638C>T	ENSP00000506089.1:n.28+19638C>T
ENST00000453660.3:n.1218C>T
ENST00000611156.4:c.*142C>T	ENSP00000483265.1:n.*142C>T
NM_020469.2:c.*142C>T	NP_065202.2:n.*142C>T
NM_020469.3:c.*142C>T	NP_065202.2:n.*142C>T