Canonical Allele Identifier: CA1882580278
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256073_133256074delinsCG , CM000671.2:g.133256073_133256074delinsCG GRCh38
NC_000009.11:g.136131460_136131461delinsCG , CM000671.1:g.136131460_136131461delinsCG GRCh37
NC_000009.10:g.135121281_135121282delinsCG NCBI36
NG_006669.1:g.21594_21595delinsCG
NG_006669.2:g.24142_24143delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.686_687delinsCG
ENST00000647353.1:n.54-4922_54-4921delinsCG
ENST00000679909.1:c.28+19088_28+19089delinsCG ENSP00000506089.1:n.28+19088_28+19089delinsCG
ENST00000453660.3:n.668_669delinsCG
ENST00000538324.2:c.654_655delinsCG ENSP00000483018.1:p.His218=
ENST00000611156.4:c.654_655delinsCG ENSP00000483265.1:p.His218=
NM_020469.2:c.657_658delinsCG NP_065202.2:p.His219=
NM_020469.3:c.657_658delinsCG NP_065202.2:p.His219=