Canonical Allele Identifier: CA1882583029
Gene: ABO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133258092C= , CM000671.2:g.133258092C= GRCh38
NC_000009.11:g.136133482C= , CM000671.1:g.136133482C= GRCh37
NC_000009.10:g.135123303C= NCBI36
NG_006669.1:g.19572G=
NG_006669.2:g.22123G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.269+5G=
ENST00000647353.1:n.54-6940G=
ENST00000651471.1:n.279G=
ENST00000679909.1:c.28+17070G= ENSP00000506089.1:n.28+17070G=
ENST00000453660.3:n.251+5G=
ENST00000538324.2:c.239+5G= ENSP00000483018.1:n.239+5G=
ENST00000611156.4:c.239+5G= ENSP00000483265.1:n.239+5G=
NM_020469.2:c.239+5G= NP_065202.2:n.239+5G=
NM_020469.3:c.239+5G= NP_065202.2:n.239+5G=
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