Canonical Allele Identifier: CA1608914033
Gene:

Linked Data

dbSNP Id: rs1759196120

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.8169820G>T , CM000668.2:g.8169820G>T GRCh38
NC_000006.11:g.8170053G>T , CM000668.1:g.8170053G>T GRCh37
NC_000006.10:g.8115052G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926440.1:n.82+11560G>T
XR_926441.1:n.189+1900G>T
XR_926442.1:n.82+11560G>T
XR_926443.1:n.82+11560G>T
XR_001743950.1:n.179+1900G>T
XR_926440.2:n.74+11560G>T
XR_926441.2:n.179+1900G>T
XR_926443.2:n.83+11560G>T