Canonical Allele Identifier: CA106421580
Gene:

Linked Data

dbSNP Id: rs913320766

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.134601447C>T , CM000666.2:g.134601447C>T GRCh38
NC_000004.11:g.135522602C>T , CM000666.1:g.135522602C>T GRCh37
NC_000004.10:g.135742052C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939212.1:n.410+14088C>T
XR_939214.1:n.392+14088C>T
XR_939214.2:n.392+14088C>T