Canonical Allele Identifier: CA2692330501
Gene: ABO HGNC NCBI

Linked Data

gnomAD v4: 9-133257280-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257280C>A , CM000671.2:g.133257280C>A GRCh38
NC_000009.11:g.136132667C>A , CM000671.1:g.136132667C>A GRCh37
NC_000009.10:g.135122488C>A NCBI36
NG_006669.1:g.20388G>T
NG_006669.2:g.22936G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.403+129G>T
ENST00000647353.1:n.54-6128G>T
ENST00000651471.1:n.329+762G>T
ENST00000679909.1:c.28+17882G>T ENSP00000506089.1:n.28+17882G>T
ENST00000453660.3:n.385+129G>T
ENST00000538324.2:c.371+129G>T ENSP00000483018.1:n.371+129G>T
ENST00000611156.4:c.371+129G>T ENSP00000483265.1:n.371+129G>T
NM_020469.2:c.374+129G>T NP_065202.2:n.374+129G>T
NM_020469.3:c.374+129G>T NP_065202.2:n.374+129G>T
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