Canonical Allele Identifier: CA727901028

Gene:

Linked Data

• dbSNP Id: rs1263141057
• MyVariant Identifiers: chr17:g.28564302C>A (hg19) ; chr17:g.30237284C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30237284C>A , CM000679.2:g.30237284C>A	GRCh38
NC_000017.10:g.28564302C>A , CM000679.1:g.28564302C>A	GRCh37
NC_000017.9:g.25588428C>A	NCBI36
NG_011747.2:g.3653G>T

Transcript Alleles

HGVS	Amino-acid Change
XR_934654.1:n.165+214C>A
XR_001752824.1:n.280+214C>A