Canonical Allele Identifier: CA973010732
Gene:

Linked Data

dbSNP Id: rs2076167687

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.94775326C>G , CM000677.2:g.94775326C>G GRCh38
NC_000015.9:g.95318555C>G , CM000677.1:g.95318555C>G GRCh37
NC_000015.8:g.93119559C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_932644.1:n.369-9309G>C
XR_932644.2:n.369-9309G>C