Canonical Allele Identifier: CA1129717093
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs1834686073
gnomAD v3: 9-133260361-A-C
gnomAD v4: 9-133260361-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133260361A>C , CM000671.2:g.133260361A>C GRCh38
NC_000009.11:g.136135764A>C , CM000671.1:g.136135764A>C GRCh37
NC_000009.10:g.135125585A>C NCBI36
NG_006669.1:g.17289T>G
NG_006669.2:g.19854T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.186-495T>G
ENST00000647353.1:n.54-9209T>G
ENST00000651471.1:n.191-495T>G
ENST00000679909.1:c.28+14801T>G ENSP00000506089.1:n.28+14801T>G
ENST00000453660.3:n.168-495T>G
ENST00000538324.2:c.156-495T>G ENSP00000483018.1:n.156-495T>G
ENST00000611156.4:c.156-495T>G ENSP00000483265.1:n.156-495T>G
NM_020469.2:c.156-495T>G NP_065202.2:n.156-495T>G
NM_020469.3:c.156-495T>G NP_065202.2:n.156-495T>G
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