Canonical Allele Identifier: CA467780409
Gene: ABO HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.136130779C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255392C>A , CM000671.2:g.133255392C>A GRCh38
NC_000009.11:g.136130779C>A , CM000671.1:g.136130779C>A GRCh37
NC_000009.10:g.135120600C>A NCBI36
NG_006669.1:g.22276G>T
NG_006669.2:g.24824G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1368G>T
ENST00000647353.1:n.54-4240G>T
ENST00000679909.1:c.28+19770G>T ENSP00000506089.1:n.28+19770G>T
ENST00000453660.3:n.1350G>T
ENST00000611156.4:c.*274G>T ENSP00000483265.1:n.*274G>T
NM_020469.2:c.*274G>T NP_065202.2:n.*274G>T
NM_020469.3:c.*274G>T NP_065202.2:n.*274G>T
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