Canonical Allele Identifier: CA259369491
Gene:

Linked Data

dbSNP Id: rs1016480852
MyVariant Identifiers: chr14:g.36854159C>T (hg19) chr14:g.36384954C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36384954C>T , CM000676.2:g.36384954C>T GRCh38
NC_000014.8:g.36854159C>T , CM000676.1:g.36854159C>T GRCh37
NC_000014.7:g.35923910C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011537428.1:c.319-12205C>T XP_011535730.1:n.319-12205C>T
XR_943756.1:n.358+23858C>T
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