Canonical Allele Identifier: CA727804431

Gene:

Linked Data

• dbSNP Id: rs1284163441
• MyVariant Identifiers: chr17:g.27703255T>C (hg19) ; chr17:g.29376237T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.29376237T>C , CM000679.2:g.29376237T>C	GRCh38
NC_000017.10:g.27703255T>C , CM000679.1:g.27703255T>C	GRCh37
NC_000017.9:g.24727381T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011525588.1:c.1008-5932A>G	XP_011523890.1:n.1008-5932A>G