Canonical Allele Identifier: CA1129715779
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs1834609045
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257089C>G , CM000671.2:g.133257089C>G GRCh38
NC_000009.11:g.136132476C>G , CM000671.1:g.136132476C>G GRCh37
NC_000009.10:g.135122297C>G NCBI36
NG_006669.1:g.20579G>C
NG_006669.2:g.23127G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.403+320G>C
ENST00000647353.1:n.54-5937G>C
ENST00000651471.1:n.330-733G>C
ENST00000679909.1:c.28+18073G>C ENSP00000506089.1:n.28+18073G>C
ENST00000453660.3:n.385+320G>C
ENST00000538324.2:c.371+320G>C ENSP00000483018.1:n.371+320G>C
ENST00000611156.4:c.371+320G>C ENSP00000483265.1:n.371+320G>C
NM_020469.2:c.374+320G>C NP_065202.2:n.374+320G>C
NM_020469.3:c.374+320G>C NP_065202.2:n.374+320G>C
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