Canonical Allele Identifier: CA467780573
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs1375108921
gnomAD v4: 9-133255411-T-C
MyVariant Identifiers: chr9:g.136130798T>C (hg19) chr9:g.133255411T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255411T>C , CM000671.2:g.133255411T>C GRCh38
NC_000009.11:g.136130798T>C , CM000671.1:g.136130798T>C GRCh37
NC_000009.10:g.135120619T>C NCBI36
NG_006669.1:g.22257A>G
NG_006669.2:g.24805A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1349A>G
ENST00000647353.1:n.54-4259A>G
ENST00000679909.1:c.28+19751A>G ENSP00000506089.1:n.28+19751A>G
ENST00000453660.3:n.1331A>G
ENST00000611156.4:c.*255A>G ENSP00000483265.1:n.*255A>G
NM_020469.2:c.*255A>G NP_065202.2:n.*255A>G
NM_020469.3:c.*255A>G NP_065202.2:n.*255A>G
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