Canonical Allele Identifier: CA375682240

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136131024G>C (hg19) ; chr9:g.133255637G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255637G>C , CM000671.2:g.133255637G>C	GRCh38
NC_000009.11:g.136131024G>C , CM000671.1:g.136131024G>C	GRCh37
NC_000009.10:g.135120845G>C	NCBI36
NG_006669.1:g.22031C>G
NG_006669.2:g.24579C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.1123C>G
ENST00000647353.1:n.54-4485C>G
ENST00000679909.1:c.28+19525C>G	ENSP00000506089.1:n.28+19525C>G
ENST00000453660.3:n.1105C>G
ENST00000538324.2:c.1087C>G	ENSP00000483018.1:p.Pro363Ala
ENST00000611156.4:c.*29C>G	ENSP00000483265.1:n.*29C>G
NM_020469.2:c.*29C>G	NP_065202.2:n.*29C>G
NM_020469.3:c.*29C>G	NP_065202.2:n.*29C>G