Canonical Allele Identifier: CA1496030111
Gene:

Linked Data

dbSNP Id: rs1728164695

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.134601435G>C , CM000666.2:g.134601435G>C GRCh38
NC_000004.11:g.135522590G>C , CM000666.1:g.135522590G>C GRCh37
NC_000004.10:g.135742040G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939212.1:n.410+14076G>C
XR_939214.1:n.392+14076G>C
XR_939214.2:n.392+14076G>C