Canonical Allele Identifier: CA261374888
Gene:

Linked Data

dbSNP Id: rs1003100063
MyVariant Identifiers: chr14:g.52884384C>T (hg19) chr14:g.52417666C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.52417666C>T , CM000676.2:g.52417666C>T GRCh38
NC_000014.8:g.52884384C>T , CM000676.1:g.52884384C>T GRCh37
NC_000014.7:g.51954134C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943866.1:n.3037G>A
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Search 100 bp 3'