Canonical Allele Identifier: CA2692330645
Gene: ABO HGNC NCBI

Linked Data

gnomAD v4: 9-133257649-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257649C>T , CM000671.2:g.133257649C>T GRCh38
NC_000009.11:g.136133036C>T , CM000671.1:g.136133036C>T GRCh37
NC_000009.10:g.135122857C>T NCBI36
NG_006669.1:g.20018G>A
NG_006669.2:g.22566G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.270-107G>A
ENST00000647353.1:n.54-6497G>A
ENST00000651471.1:n.329+393G>A
ENST00000679909.1:c.28+17513G>A ENSP00000506089.1:n.28+17513G>A
ENST00000453660.3:n.252-107G>A
ENST00000538324.2:c.240-107G>A ENSP00000483018.1:n.240-107G>A
ENST00000611156.4:c.240-107G>A ENSP00000483265.1:n.240-107G>A
NM_020469.2:c.240-107G>A NP_065202.2:n.240-107G>A
NM_020469.3:c.240-107G>A NP_065202.2:n.240-107G>A
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