Canonical Allele Identifier: CA2581689797
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94587797T>C , CM000663.2:g.94587797T>C GRCh38
NC_000001.10:g.95053353T>C , CM000663.1:g.95053353T>C GRCh37
NC_000001.9:g.94825941T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001738161.1:n.461+24184T>C