Canonical Allele Identifier: CA375682192

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136130997A>C (hg19) ; chr9:g.133255610A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255610A>C , CM000671.2:g.133255610A>C	GRCh38
NC_000009.11:g.136130997A>C , CM000671.1:g.136130997A>C	GRCh37
NC_000009.10:g.135120818A>C	NCBI36
NG_006669.1:g.22058T>G
NG_006669.2:g.24606T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.1150T>G
ENST00000647353.1:n.54-4458T>G
ENST00000679909.1:c.28+19552T>G	ENSP00000506089.1:n.28+19552T>G
ENST00000453660.3:n.1132T>G
ENST00000538324.2:c.1114T>G	ENSP00000483018.1:p.Trp372Gly
ENST00000611156.4:c.*56T>G	ENSP00000483265.1:n.*56T>G
NM_020469.2:c.*56T>G	NP_065202.2:n.*56T>G
NM_020469.3:c.*56T>G	NP_065202.2:n.*56T>G