Canonical Allele Identifier: CA375686133
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs1273200931
MyVariant Identifiers: chr9:g.136131564G>C (hg19) chr9:g.133256177G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256177G>C , CM000671.2:g.133256177G>C GRCh38
NC_000009.11:g.136131564G>C , CM000671.1:g.136131564G>C GRCh37
NC_000009.10:g.135121385G>C NCBI36
NG_006669.1:g.21491C>G
NG_006669.2:g.24039C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.583C>G
ENST00000647353.1:n.54-5025C>G
ENST00000651471.1:n.509C>G
ENST00000679909.1:c.28+18985C>G ENSP00000506089.1:n.28+18985C>G
ENST00000453660.3:n.565C>G
ENST00000538324.2:c.551C>G ENSP00000483018.1:p.Ser184Cys
ENST00000611156.4:c.551C>G ENSP00000483265.1:p.Ser184Cys
NM_020469.2:c.554C>G NP_065202.2:p.Ser185Cys
NM_020469.3:c.554C>G NP_065202.2:p.Ser185Cys
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