Canonical Allele Identifier: CA200766323
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs952029831
MyVariant Identifiers: chr9:g.136133290C>T (hg19) chr9:g.133257903C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257903C>T , CM000671.2:g.133257903C>T GRCh38
NC_000009.11:g.136133290C>T , CM000671.1:g.136133290C>T GRCh37
NC_000009.10:g.135123111C>T NCBI36
NG_006669.1:g.19764G>A
NG_006669.2:g.22312G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.269+194G>A
ENST00000647353.1:n.54-6751G>A
ENST00000651471.1:n.329+139G>A
ENST00000679909.1:c.28+17259G>A ENSP00000506089.1:n.28+17259G>A
ENST00000453660.3:n.251+194G>A
ENST00000538324.2:c.239+194G>A ENSP00000483018.1:n.239+194G>A
ENST00000611156.4:c.239+194G>A ENSP00000483265.1:n.239+194G>A
NM_020469.2:c.239+194G>A NP_065202.2:n.239+194G>A
NM_020469.3:c.239+194G>A NP_065202.2:n.239+194G>A
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