Canonical Allele Identifier: CA1882579937
Gene: ABO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255936_133255937delinsGT , CM000671.2:g.133255936_133255937delinsGT GRCh38
NC_000009.11:g.136131323_136131324delinsGT , CM000671.1:g.136131323_136131324delinsGT GRCh37
NC_000009.10:g.135121144_135121145delinsGT NCBI36
NG_006669.1:g.21731_21732delinsAC
NG_006669.2:g.24279_24280delinsAC

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.823_824delinsAC
ENST00000647353.1:n.54-4785_54-4784delinsAC
ENST00000679909.1:c.28+19225_28+19226delinsAC ENSP00000506089.1:n.28+19225_28+19226deli...
ENST00000453660.3:n.805_806delinsAC
ENST00000538324.2:c.791_792delinsAC ENSP00000483018.1:p.Tyr264=
ENST00000611156.4:c.791_792delinsAC ENSP00000483265.1:p.Tyr264=
NM_020469.2:c.794_795delinsAC NP_065202.2:p.Tyr265=
NM_020469.3:c.794_795delinsAC NP_065202.2:p.Tyr265=
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