Canonical Allele Identifier: CA1496030120
Gene:

Linked Data

dbSNP Id: rs1728164838

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.134601441C>G , CM000666.2:g.134601441C>G GRCh38
NC_000004.11:g.135522596C>G , CM000666.1:g.135522596C>G GRCh37
NC_000004.10:g.135742046C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939212.1:n.410+14082C>G
XR_939214.1:n.392+14082C>G
XR_939214.2:n.392+14082C>G