Canonical Allele Identifier: CA1502607443
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.148748472T= , CM000666.2:g.148748472T= GRCh38
NC_000004.11:g.149669624T= , CM000666.1:g.149669624T= GRCh37
NC_000004.10:g.149889074T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001741441.1:n.1746-118285T=