Canonical Allele Identifier: CA1608914046
Gene:

Linked Data

dbSNP Id: rs1003569981

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.8169826C>T , CM000668.2:g.8169826C>T GRCh38
NC_000006.11:g.8170059C>T , CM000668.1:g.8170059C>T GRCh37
NC_000006.10:g.8115058C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926440.1:n.82+11566C>T
XR_926441.1:n.189+1906C>T
XR_926442.1:n.82+11566C>T
XR_926443.1:n.82+11566C>T
XR_001743950.1:n.179+1906C>T
XR_926440.2:n.74+11566C>T
XR_926441.2:n.179+1906C>T
XR_926443.2:n.83+11566C>T