Canonical Allele Identifier: CA2692330441
Gene: ABO HGNC NCBI

Linked Data

gnomAD v4: 9-133256473-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256473C>T , CM000671.2:g.133256473C>T GRCh38
NC_000009.11:g.136131860C>T , CM000671.1:g.136131860C>T GRCh37
NC_000009.10:g.135121681C>T NCBI36
NG_006669.1:g.21195G>A
NG_006669.2:g.23743G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.404-117G>A
ENST00000647353.1:n.54-5321G>A
ENST00000651471.1:n.330-117G>A
ENST00000679909.1:c.28+18689G>A ENSP00000506089.1:n.28+18689G>A
ENST00000453660.3:n.386-117G>A
ENST00000538324.2:c.372-117G>A ENSP00000483018.1:n.372-117G>A
ENST00000611156.4:c.372-117G>A ENSP00000483265.1:n.372-117G>A
NM_020469.2:c.375-117G>A NP_065202.2:n.375-117G>A
NM_020469.3:c.375-117G>A NP_065202.2:n.375-117G>A
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