Canonical Allele Identifier: CA375686279

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136131642A>C (hg19) ; chr9:g.133256255A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256255A>C , CM000671.2:g.133256255A>C	GRCh38
NC_000009.11:g.136131642A>C , CM000671.1:g.136131642A>C	GRCh37
NC_000009.10:g.135121463A>C	NCBI36
NG_006669.1:g.21413T>G
NG_006669.2:g.23961T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.505T>G
ENST00000647353.1:n.54-5103T>G
ENST00000651471.1:n.431T>G
ENST00000679909.1:c.28+18907T>G	ENSP00000506089.1:n.28+18907T>G
ENST00000453660.3:n.487T>G
ENST00000538324.2:c.473T>G	ENSP00000483018.1:p.Val158Gly
ENST00000611156.4:c.473T>G	ENSP00000483265.1:p.Val158Gly
NM_020469.2:c.476T>G	NP_065202.2:p.Val159Gly
NM_020469.3:c.476T>G	NP_065202.2:p.Val159Gly