Canonical Allele Identifier: CA2720592099

Gene:

Linked Data

• dbSNP Id: rs2119114471

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.129576864T>C , CM000671.2:g.129576864T>C	GRCh38
NC_000009.11:g.132339143T>C , CM000671.1:g.132339143T>C	GRCh37
NC_000009.10:g.131378964T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_930390.1:n.182+1266T>C