Canonical Allele Identifier: CA1608931651
Gene:

Linked Data

dbSNP Id: rs1760012751

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.8228656T>C , CM000668.2:g.8228656T>C GRCh38
NC_000006.11:g.8228889T>C , CM000668.1:g.8228889T>C GRCh37
NC_000006.10:g.8173888T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926440.1:n.83-1458T>C
XR_926441.1:n.190-10275T>C
XR_926442.1:n.83-1458T>C
XR_926443.1:n.83-10275T>C
XR_001743950.1:n.180-10275T>C
XR_926440.2:n.75-1458T>C
XR_926441.2:n.180-10275T>C
XR_926443.2:n.84-10275T>C