Canonical Allele Identifier: CA1714659123
Community Standard Title: NC_000007.14:g.67594280T=
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.67594280T= , CM000669.2:g.67594280T= GRCh38
NC_000007.13:g.67059267T= , CM000669.1:g.67059267T= GRCh37
NC_000007.12:g.66696702T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001745238.2:n.163+8031A=