Canonical Allele Identifier: CA1496030187
Gene:

Linked Data

dbSNP Id: rs1728166465

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.134601600C>T , CM000666.2:g.134601600C>T GRCh38
NC_000004.11:g.135522755C>T , CM000666.1:g.135522755C>T GRCh37
NC_000004.10:g.135742205C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939212.1:n.410+14241C>T
XR_939214.1:n.392+14241C>T
XR_939214.2:n.392+14241C>T