Canonical Allele Identifier: CA375686677

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136132868T>C (hg19) ; chr9:g.133257481T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133257481T>C , CM000671.2:g.133257481T>C	GRCh38
NC_000009.11:g.136132868T>C , CM000671.1:g.136132868T>C	GRCh37
NC_000009.10:g.135122689T>C	NCBI36
NG_006669.1:g.20187A>G
NG_006669.2:g.22735A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.331A>G
ENST00000647353.1:n.54-6329A>G
ENST00000651471.1:n.329+561A>G
ENST00000679909.1:c.28+17681A>G	ENSP00000506089.1:n.28+17681A>G
ENST00000453660.3:n.313A>G
ENST00000538324.2:c.299A>G	ENSP00000483018.1:p.Asn100Ser
ENST00000611156.4:c.299A>G	ENSP00000483265.1:p.Asn100Ser
NM_020469.2:c.302A>G	NP_065202.2:p.Asn101Ser
NM_020469.3:c.302A>G	NP_065202.2:p.Asn101Ser