Canonical Allele Identifier: CA1608913810
Gene:

Linked Data

dbSNP Id: rs1759192285

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.8169582C>T , CM000668.2:g.8169582C>T GRCh38
NC_000006.11:g.8169815C>T , CM000668.1:g.8169815C>T GRCh37
NC_000006.10:g.8114814C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926440.1:n.82+11322C>T
XR_926441.1:n.189+1662C>T
XR_926442.1:n.82+11322C>T
XR_926443.1:n.82+11322C>T
XR_001743950.1:n.179+1662C>T
XR_926440.2:n.74+11322C>T
XR_926441.2:n.179+1662C>T
XR_926443.2:n.83+11322C>T