Canonical Allele Identifier: CA2276822021
Gene: C17orf99 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.78146086C= , CM000679.2:g.78146086C= GRCh38
NC_000017.10:g.76142167C= , CM000679.1:g.76142167C= GRCh37
NC_000017.9:g.73653762C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011524152.1:c.-6C= XP_011522454.1:n.-6C=
XM_011524152.2:c.-6C= XP_011522454.1:n.-6C=
XM_017023997.1:c.-6C= XP_016879486.1:n.-6C=