Canonical Allele Identifier: CA375686308

Gene: ABO

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256268G>C , CM000671.2:g.133256268G>C	GRCh38
NC_000009.11:g.136131655G>C , CM000671.1:g.136131655G>C	GRCh37
NC_000009.10:g.135121476G>C	NCBI36
NG_006669.1:g.21400C>G
NG_006669.2:g.23948C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.492C>G
ENST00000647353.1:n.54-5116C>G
ENST00000651471.1:n.418C>G
ENST00000679909.1:c.28+18894C>G	ENSP00000506089.1:n.28+18894C>G
ENST00000453660.3:n.474C>G
ENST00000538324.2:c.460C>G	ENSP00000483018.1:p.Gln154Glu
ENST00000611156.4:c.460C>G	ENSP00000483265.1:p.Gln154Glu
NM_020469.2:c.463C>G	NP_065202.2:p.Gln155Glu
NM_020469.3:c.463C>G	NP_065202.2:p.Gln155Glu