Canonical Allele Identifier: CA2517633097
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.99817262A>G , CM000677.2:g.99817262A>G GRCh38
NC_000015.9:g.100357467A>G , CM000677.1:g.100357467A>G GRCh37
NC_000015.8:g.98174990A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_932717.1:n.408+4176A>G
XR_932718.1:n.408+4176A>G
XR_932719.1:n.514+8960A>G
XR_932720.1:n.409-1676A>G
NR_135737.1:n.346+4176A>G