Canonical Allele Identifier: CA1181633469
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94564036T= , CM000663.2:g.94564036T= GRCh38
NC_000001.10:g.95029592T= , CM000663.1:g.95029592T= GRCh37
NC_000001.9:g.94802180T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001738161.1:n.461+423T=