Canonical Allele Identifier: CA375686176

Gene: ABO

Linked Data

• dbSNP Id: rs1834578009
• MyVariant Identifiers: chr9:g.136131583T>C (hg19) ; chr9:g.133256196T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256196T>C , CM000671.2:g.133256196T>C	GRCh38
NC_000009.11:g.136131583T>C , CM000671.1:g.136131583T>C	GRCh37
NC_000009.10:g.135121404T>C	NCBI36
NG_006669.1:g.21472A>G
NG_006669.2:g.24020A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.564A>G
ENST00000647353.1:n.54-5044A>G
ENST00000651471.1:n.490A>G
ENST00000679909.1:c.28+18966A>G	ENSP00000506089.1:n.28+18966A>G
ENST00000453660.3:n.546A>G
ENST00000538324.2:c.532A>G	ENSP00000483018.1:p.Lys178Glu
ENST00000611156.4:c.532A>G	ENSP00000483265.1:p.Lys178Glu
NM_020469.2:c.535A>G	NP_065202.2:p.Lys179Glu
NM_020469.3:c.535A>G	NP_065202.2:p.Lys179Glu