Canonical Allele Identifier: CA259369484
Gene:

Linked Data

dbSNP Id: rs918421976
MyVariant Identifiers: chr14:g.36854135T>A (hg19) chr14:g.36384930T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36384930T>A , CM000676.2:g.36384930T>A GRCh38
NC_000014.8:g.36854135T>A , CM000676.1:g.36854135T>A GRCh37
NC_000014.7:g.35923886T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011537428.1:c.319-12229T>A XP_011535730.1:n.319-12229T>A
XR_943756.1:n.358+23834T>A
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