Canonical Allele Identifier: CA14469474

Gene: C17orf99

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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