Canonical Allele Identifier: CA591308928
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs1250501842
gnomAD v2: 9-136132419-A-G
gnomAD v3: 9-133257032-A-G
gnomAD v4: 9-133257032-A-G
MyVariant Identifiers: chr9:g.136132419A>G (hg19) chr9:g.133257032A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257032A>G , CM000671.2:g.133257032A>G GRCh38
NC_000009.11:g.136132419A>G , CM000671.1:g.136132419A>G GRCh37
NC_000009.10:g.135122240A>G NCBI36
NG_006669.1:g.20636T>C
NG_006669.2:g.23184T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.403+377T>C
ENST00000647353.1:n.54-5880T>C
ENST00000651471.1:n.330-676T>C
ENST00000679909.1:c.28+18130T>C ENSP00000506089.1:n.28+18130T>C
ENST00000453660.3:n.385+377T>C
ENST00000538324.2:c.371+377T>C ENSP00000483018.1:n.371+377T>C
ENST00000611156.4:c.371+377T>C ENSP00000483265.1:n.371+377T>C
NM_020469.2:c.374+377T>C NP_065202.2:n.374+377T>C
NM_020469.3:c.374+377T>C NP_065202.2:n.374+377T>C
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