Canonical Allele Identifier: CA1462694316
Gene:

Linked Data

dbSNP Id: rs1454791540

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62558307G>C , CM000666.2:g.62558307G>C GRCh38
NC_000004.11:g.63424025G>C , CM000666.1:g.63424025G>C GRCh37
NC_000004.10:g.63106620G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_938814.1:n.161-5537G>C