Canonical Allele Identifier: CA1502607321
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.148748429T= , CM000666.2:g.148748429T= GRCh38
NC_000004.11:g.149669581T= , CM000666.1:g.149669581T= GRCh37
NC_000004.10:g.149889031T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001741441.1:n.1746-118328T=