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Canonical Allele Identifier:
CA375685071
Community Standard Title: NC_000009.12:g.133255928C>T
Gene: ABO
HGNC
NCBI
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.133255928C>T , CM000671.2:g.133255928C>T
GRCh38
NC_000009.11:g.136131315C>T , CM000671.1:g.136131315C>T
GRCh37
NC_000009.10:g.135121136C>T
NCBI36
NG_006669.1:g.21740G>A
NG_006669.2:g.24288G>A
Transcript Alleles
HGVS
Amino-acid Change
NM_020469.2:c.803G>A
NP_065202.2:p.Gly268Glu
NM_020469.3:c.803G>A
NP_065202.2:p.Gly268Glu
ENST00000453660.3:n.814G>A
ENST00000453660.4:n.832G>A
ENST00000538324.2:c.800G>A
ENSP00000483018.1:p.Gly267Glu
ENST00000611156.4:c.800G>A
ENSP00000483265.1:p.Gly267Glu
ENST00000647353.1:n.54-4776G>A
ENST00000679909.1:c.28+19234G>A
ENSP00000506089.1:n.28+19234G>A
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