Canonical Allele Identifier: CA190667298
Gene:

Linked Data

dbSNP Id: rs964386837
MyVariant Identifiers: chr9:g.21755954A>T (hg19) chr9:g.21755955A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21755955A>T , CM000671.2:g.21755955A>T GRCh38
NC_000009.11:g.21755954A>T , CM000671.1:g.21755954A>T GRCh37
NC_000009.10:g.21745954A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001746563.2:n.163+11870T>A
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