Canonical Allele Identifier: CA1468603713

Gene:

Linked Data

• dbSNP Id: rs1750547367

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.74304443T>C , CM000666.2:g.74304443T>C	GRCh38
NC_000004.11:g.75170160T>C , CM000666.1:g.75170160T>C	GRCh37
NC_000004.10:g.75389024T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_938877.1:n.120-25665A>G
XR_938877.2:n.126-25665A>G