Canonical Allele Identifier: CA275962872
Gene:

Linked Data

dbSNP Id: rs369857812

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.94775362T>C , CM000677.2:g.94775362T>C GRCh38
NC_000015.9:g.95318591T>C , CM000677.1:g.95318591T>C GRCh37
NC_000015.8:g.93119595T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_932644.1:n.369-9345A>G
XR_932644.2:n.369-9345A>G