Canonical Allele Identifier: CA1496030099
Gene:

Linked Data

dbSNP Id: rs1728164514

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.134601419G>A , CM000666.2:g.134601419G>A GRCh38
NC_000004.11:g.135522574G>A , CM000666.1:g.135522574G>A GRCh37
NC_000004.10:g.135742024G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939212.1:n.410+14060G>A
XR_939214.1:n.392+14060G>A
XR_939214.2:n.392+14060G>A