Canonical Allele Identifier: CA2181824883
Community Standard Title: NC_000015.10:g.61708933A=
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.61708933A= , CM000677.2:g.61708933A= GRCh38
NC_000015.9:g.62001132A= , CM000677.1:g.62001132A= GRCh37
NC_000015.8:g.59788424A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001751569.1:n.77+6182T=