Canonical Allele Identifier: CA1502607163
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.148748298T= , CM000666.2:g.148748298T= GRCh38
NC_000004.11:g.149669450T= , CM000666.1:g.149669450T= GRCh37
NC_000004.10:g.149888900T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001741441.1:n.1746-118459T=