Canonical Allele Identifier: CA276104120

Gene:

Linked Data

• dbSNP Id: rs954881247
• MyVariant Identifiers: chr15:g.96325585T>C (hg19) ; chr15:g.95782356T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.95782356T>C , CM000677.2:g.95782356T>C	GRCh38
NC_000015.9:g.96325585T>C , CM000677.1:g.96325585T>C	GRCh37
NC_000015.8:g.94126589T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_932654.1:n.148-42833T>C