Canonical Allele Identifier: CA467781951

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136130985T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255598T>C , CM000671.2:g.133255598T>C	GRCh38
NC_000009.11:g.136130985T>C , CM000671.1:g.136130985T>C	GRCh37
NC_000009.10:g.135120806T>C	NCBI36
NG_006669.1:g.22070A>G
NG_006669.2:g.24618A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.1162A>G
ENST00000647353.1:n.54-4446A>G
ENST00000679909.1:c.28+19564A>G	ENSP00000506089.1:n.28+19564A>G
ENST00000453660.3:n.1144A>G
ENST00000611156.4:c.*68A>G	ENSP00000483265.1:n.*68A>G
NM_020469.2:c.*68A>G	NP_065202.2:n.*68A>G
NM_020469.3:c.*68A>G	NP_065202.2:n.*68A>G