Canonical Allele Identifier: CA260835464
Gene:

Linked Data

dbSNP Id: rs955313938
MyVariant Identifiers: chr14:g.51323590C>T (hg19) chr14:g.50856872C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50856872C>T , CM000676.2:g.50856872C>T GRCh38
NC_000014.8:g.51323590C>T , CM000676.1:g.51323590C>T GRCh37
NC_000014.7:g.50393340C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943848.1:n.282+1226G>A
XR_943848.2:n.643+1226G>A
Search 100 bp 5'
Search 100 bp 3'