Canonical Allele Identifier: CA797158712
Gene:

Linked Data

dbSNP Id: rs1168845176

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62558284C>T , CM000666.2:g.62558284C>T GRCh38
NC_000004.11:g.63424002C>T , CM000666.1:g.63424002C>T GRCh37
NC_000004.10:g.63106597C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_938814.1:n.161-5560C>T