Canonical Allele Identifier: CA190667406
Gene:

Linked Data

dbSNP Id: rs962251195
MyVariant Identifiers: chr9:g.21756063G>T (hg19) chr9:g.21756064G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21756064G>T , CM000671.2:g.21756064G>T GRCh38
NC_000009.11:g.21756063G>T , CM000671.1:g.21756063G>T GRCh37
NC_000009.10:g.21746063G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001746563.2:n.163+11761C>A
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