Canonical Allele Identifier: CA2485976202
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.213682250T= , CM000663.2:g.213682250T= GRCh38
NC_000001.10:g.213855593T= , CM000663.1:g.213855593T= GRCh37
NC_000001.9:g.211922216T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001738463.1:n.601-49167T=
XR_001738464.1:n.426-49167T=