Canonical Allele Identifier: CA1605276874
Gene:

Linked Data

dbSNP Id: rs1287379841

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.465923C>T , CM000668.2:g.465923C>T GRCh38
NC_000006.11:g.465923C>T , CM000668.1:g.465923C>T GRCh37
NC_000006.10:g.410923C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926364.1:n.2714+12198C>T
XR_926365.1:n.2548+12198C>T
XR_001743914.1:n.482-9285C>T