Canonical Allele Identifier: CA2485976199
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.213682246T= , CM000663.2:g.213682246T= GRCh38
NC_000001.10:g.213855589T= , CM000663.1:g.213855589T= GRCh37
NC_000001.9:g.211922212T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001738463.1:n.601-49171T=
XR_001738464.1:n.426-49171T=