Canonical Allele Identifier: CA274976207
Gene:

Linked Data

dbSNP Id: rs892586844
MyVariant Identifiers: chr15:g.87695415T>C (hg19) chr15:g.87152184T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.87152184T>C , CM000677.2:g.87152184T>C GRCh38
NC_000015.9:g.87695415T>C , CM000677.1:g.87695415T>C GRCh37
NC_000015.8:g.85496419T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_932582.1:n.167-26043T>C
XR_932582.2:n.167-26043T>C
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Search 100 bp 3'