Canonical Allele Identifier: CA467779972
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs62641787
gnomAD v2: 9-136130686-C-T
gnomAD v3: 9-133255299-C-T
gnomAD v4: 9-133255299-C-T
MyVariant Identifiers: chr9:g.136130686C>T (hg19) chr9:g.133255299C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255299C>T , CM000671.2:g.133255299C>T GRCh38
NC_000009.11:g.136130686C>T , CM000671.1:g.136130686C>T GRCh37
NC_000009.10:g.135120507C>T NCBI36
NG_006669.1:g.22369G>A
NG_006669.2:g.24917G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1461G>A
ENST00000647353.1:n.54-4147G>A
ENST00000679909.1:c.28+19863G>A ENSP00000506089.1:n.28+19863G>A
ENST00000453660.3:n.1443G>A
ENST00000611156.4:c.*367G>A ENSP00000483265.1:n.*367G>A
NM_020469.2:c.*367G>A NP_065202.2:n.*367G>A
NM_020469.3:c.*367G>A NP_065202.2:n.*367G>A
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