Canonical Allele Identifier: CA375684925

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136131294T>G (hg19) ; chr9:g.133255907T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255907T>G , CM000671.2:g.133255907T>G	GRCh38
NC_000009.11:g.136131294T>G , CM000671.1:g.136131294T>G	GRCh37
NC_000009.10:g.135121115T>G	NCBI36
NG_006669.1:g.21761A>C
NG_006669.2:g.24309A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.853A>C
ENST00000647353.1:n.54-4755A>C
ENST00000679909.1:c.28+19255A>C	ENSP00000506089.1:n.28+19255A>C
ENST00000453660.3:n.835A>C
ENST00000538324.2:c.821A>C	ENSP00000483018.1:p.Gln274Pro
ENST00000611156.4:c.821A>C	ENSP00000483265.1:p.Gln274Pro
NM_020469.2:c.824A>C	NP_065202.2:p.Gln275Pro
NM_020469.3:c.824A>C	NP_065202.2:p.Gln275Pro