Canonical Allele Identifier: CA467784724
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs587631714
gnomAD v3: 9-133261746-C-T
gnomAD v4: 9-133261746-C-T
MyVariant Identifiers: chr9:g.136137149C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133261746C>T , CM000671.2:g.133261746C>T GRCh38
NC_000009.11:g.136137149C>T , CM000671.1:g.136137149C>T GRCh37
NC_000009.10:g.135126970C>T NCBI36
NG_006669.1:g.15904G>A
NG_006669.2:g.18469G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.128+353G>A
ENST00000647353.1:n.54-10594G>A
ENST00000651471.1:n.133+353G>A
ENST00000679909.1:c.28+13416G>A ENSP00000506089.1:n.28+13416G>A
ENST00000453660.3:n.110+353G>A
ENST00000538324.2:c.98+353G>A ENSP00000483018.1:n.98+353G>A
ENST00000611156.4:c.98+353G>A ENSP00000483265.1:n.98+353G>A
NM_020469.2:c.98+353G>A NP_065202.2:n.98+353G>A
NM_020469.3:c.98+353G>A NP_065202.2:n.98+353G>A
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