Canonical Allele Identifier: CA1496030108
Gene:

Linked Data

dbSNP Id: rs1728164644

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.134601427T>C , CM000666.2:g.134601427T>C GRCh38
NC_000004.11:g.135522582T>C , CM000666.1:g.135522582T>C GRCh37
NC_000004.10:g.135742032T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939212.1:n.410+14068T>C
XR_939214.1:n.392+14068T>C
XR_939214.2:n.392+14068T>C