Canonical Allele Identifier: CA1496030115
Gene:

Linked Data

dbSNP Id: rs1728164716

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.134601437C>T , CM000666.2:g.134601437C>T GRCh38
NC_000004.11:g.135522592C>T , CM000666.1:g.135522592C>T GRCh37
NC_000004.10:g.135742042C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939212.1:n.410+14078C>T
XR_939214.1:n.392+14078C>T
XR_939214.2:n.392+14078C>T