Canonical Allele Identifier: CA291560769

Gene:

Linked Data

• dbSNP Id: rs925035566
• MyVariant Identifiers: chr17:g.50211623C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50211623C>T , CM000679.2:g.50211623C>T	GRCh38
NC_000017.10:g.48288984C>T , CM000679.1:g.48288984C>T	GRCh37
NC_000017.9:g.45643983C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_934838.1:n.43-2212C>T