Canonical Allele Identifier: CA375684342

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136131216T>G (hg19) ; chr9:g.133255829T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255829T>G , CM000671.2:g.133255829T>G	GRCh38
NC_000009.11:g.136131216T>G , CM000671.1:g.136131216T>G	GRCh37
NC_000009.10:g.135121037T>G	NCBI36
NG_006669.1:g.21839A>C
NG_006669.2:g.24387A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.931A>C
ENST00000647353.1:n.54-4677A>C
ENST00000679909.1:c.28+19333A>C	ENSP00000506089.1:n.28+19333A>C
ENST00000453660.3:n.913A>C
ENST00000538324.2:c.899A>C	ENSP00000483018.1:p.His300Pro
ENST00000611156.4:c.899A>C	ENSP00000483265.1:p.His300Pro
NM_020469.2:c.902A>C	NP_065202.2:p.His301Pro
NM_020469.3:c.902A>C	NP_065202.2:p.His301Pro