Canonical Allele Identifier: CA1704517811
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.46033028T= , CM000669.2:g.46033028T= GRCh38
NC_000007.13:g.46072626T= , CM000669.1:g.46072626T= GRCh37
NC_000007.12:g.46039151T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001745203.1:n.1270-3590T=