Canonical Allele Identifier: CA860763654
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs1412429381
gnomAD v3: 9-133274058-C-T
gnomAD v4: 9-133274058-C-T
MyVariant Identifiers: chr9:g.133274058C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133274058C>T , CM000671.2:g.133274058C>T GRCh38
NC_000009.11:g.136149474C>T , CM000671.1:g.136149474C>T GRCh37
NC_000009.10:g.135139295C>T NCBI36
NG_006669.1:g.3577G>A
NG_006669.2:g.6157G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.58+1104G>A
ENST00000647353.1:n.53+1104G>A
ENST00000651471.1:n.63+1904G>A
ENST00000679909.1:c.28+1104G>A ENSP00000506089.1:n.28+1104G>A
ENST00000453660.3:n.40+1104G>A
ENST00000538324.2:c.28+1104G>A ENSP00000483018.1:n.28+1104G>A
ENST00000611156.4:c.28+1104G>A ENSP00000483265.1:n.28+1104G>A
NM_020469.2:c.28+1104G>A NP_065202.2:n.28+1104G>A
NM_020469.3:c.28+1104G>A NP_065202.2:n.28+1104G>A
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