Canonical Allele Identifier: CA1605276810
Gene:

Linked Data

dbSNP Id: rs543600521

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.465832G>C , CM000668.2:g.465832G>C GRCh38
NC_000006.11:g.465832G>C , CM000668.1:g.465832G>C GRCh37
NC_000006.10:g.410832G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926364.1:n.2714+12107G>C
XR_926365.1:n.2548+12107G>C
XR_001743914.1:n.482-9376G>C