Canonical Allele Identifier: CA1605795014
Gene:

Linked Data

dbSNP Id: rs9378636

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1535660C>G , CM000668.2:g.1535660C>G GRCh38
NC_000006.11:g.1535895C>G , CM000668.1:g.1535895C>G GRCh37
NC_000006.10:g.1480894C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_427861.2:n.234+16686G>C
XR_926380.1:n.218-2796C>G
XR_926381.1:n.1108-2796C>G
XR_926382.1:n.235-6481G>C
XR_926384.1:n.200-6481G>C
XR_001743921.1:n.235-6505G>C
XR_427861.3:n.234+16686G>C
XR_926381.2:n.1123-2796C>G