Canonical Allele Identifier: CA134548290
Gene:

Linked Data

dbSNP Id: rs987664087

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.8169752C>T , CM000668.2:g.8169752C>T GRCh38
NC_000006.11:g.8169985C>T , CM000668.1:g.8169985C>T GRCh37
NC_000006.10:g.8114984C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926440.1:n.82+11492C>T
XR_926441.1:n.189+1832C>T
XR_926442.1:n.82+11492C>T
XR_926443.1:n.82+11492C>T
XR_001743950.1:n.179+1832C>T
XR_926440.2:n.74+11492C>T
XR_926441.2:n.179+1832C>T
XR_926443.2:n.83+11492C>T