Canonical Allele Identifier: CA8609177

Gene: KIF18B

Linked Data

• dbSNP Id: rs781237000
• ExAC: 17:43003495 C / T
• gnomAD v2: 17-43003495-C-T
• gnomAD v3: 17-44926127-C-T
• gnomAD v4: 17-44926127-C-T
• MyVariant Identifiers: chr17:g.43003495C>T (hg19) ; chr17:g.44926127C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44926127C>T , CM000679.2:g.44926127C>T	GRCh38
NC_000017.10:g.43003495C>T , CM000679.1:g.43003495C>T	GRCh37
NC_000017.9:g.40359021C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593135.6:c.2512G>A MANE Select	ENSP00000465992.1:p.Val838Met
ENST00000587309.5:c.*273G>A	ENSP00000465377.1:n.*273G>A
ENST00000593135.5:c.2512G>A	ENSP00000465992.1:p.Val838Met
NM_001264573.1:c.*273G>A	NP_001251503.1:n.*273G>A
NM_001265577.1:c.2512G>A	NP_001252506.1:p.Val838Met
XM_011524385.1:c.2575G>A	XP_011522687.1:p.Val859Met
XM_011524386.1:c.2548G>A	XP_011522688.1:p.Val850Met
XM_011524387.1:c.2548G>A	XP_011522689.1:p.Val850Met
XM_011524388.1:c.2539G>A	XP_011522690.1:p.Val847Met
XM_011524389.1:c.*273G>A	XP_011522691.1:n.*273G>A
XM_011524390.1:c.2470G>A	XP_011522692.1:p.Val824Met
XM_011524385.2:c.2575G>A	XP_011522687.1:p.Val859Met
XM_011524386.2:c.2548G>A	XP_011522688.1:p.Val850Met
XM_011524387.2:c.2548G>A	XP_011522689.1:p.Val850Met
XM_011524388.3:c.2539G>A	XP_011522690.1:p.Val847Met
XM_011524389.2:c.*273G>A	XP_011522691.1:n.*273G>A
XM_011524390.2:c.2470G>A	XP_011522692.1:p.Val824Met
NM_001264573.2:c.*273G>A	NP_001251503.1:n.*273G>A
NM_001265577.2:c.2512G>A MANE Select	NP_001252506.1:p.Val838Met