Canonical Allele Identifier: CA375684487

Gene: ABO

Linked Data

• COSMIC: COSM5747089
• MyVariant Identifiers: chr9:g.136131234C>T (hg19) ; chr9:g.133255847C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255847C>T , CM000671.2:g.133255847C>T	GRCh38
NC_000009.11:g.136131234C>T , CM000671.1:g.136131234C>T	GRCh37
NC_000009.10:g.135121055C>T	NCBI36
NG_006669.1:g.21821G>A
NG_006669.2:g.24369G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.913G>A
ENST00000647353.1:n.54-4695G>A
ENST00000679909.1:c.28+19315G>A	ENSP00000506089.1:n.28+19315G>A
ENST00000453660.3:n.895G>A
ENST00000538324.2:c.881G>A	ENSP00000483018.1:p.Gly294Asp
ENST00000611156.4:c.881G>A	ENSP00000483265.1:p.Gly294Asp
NM_020469.2:c.884G>A	NP_065202.2:p.Gly295Asp
NM_020469.3:c.884G>A	NP_065202.2:p.Gly295Asp