Canonical Allele Identifier: CA1181633466
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94564031T= , CM000663.2:g.94564031T= GRCh38
NC_000001.10:g.95029587T= , CM000663.1:g.95029587T= GRCh37
NC_000001.9:g.94802175T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001738161.1:n.461+418T=