Canonical Allele Identifier: CA1882581993
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs1834607742
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257052C>T , CM000671.2:g.133257052C>T GRCh38
NC_000009.11:g.136132439C>T , CM000671.1:g.136132439C>T GRCh37
NC_000009.10:g.135122260C>T NCBI36
NG_006669.1:g.20616G>A
NG_006669.2:g.23164G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.403+357G>A
ENST00000647353.1:n.54-5900G>A
ENST00000651471.1:n.330-696G>A
ENST00000679909.1:c.28+18110G>A ENSP00000506089.1:n.28+18110G>A
ENST00000453660.3:n.385+357G>A
ENST00000538324.2:c.371+357G>A ENSP00000483018.1:n.371+357G>A
ENST00000611156.4:c.371+357G>A ENSP00000483265.1:n.371+357G>A
NM_020469.2:c.374+357G>A NP_065202.2:n.374+357G>A
NM_020469.3:c.374+357G>A NP_065202.2:n.374+357G>A
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