Canonical Allele Identifier: CA14379584

Gene: KIF18B

Linked Data

• dbSNP Id: rs736866
• gnomAD v2: 17-43009797-C-A
• gnomAD v3: 17-44932429-C-A
• gnomAD v4: 17-44932429-C-A
• MyVariant Identifiers: chr17:g.43009797C>A (hg19) ; chr17:g.44932429C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44932429C>A , CM000679.2:g.44932429C>A	GRCh38
NC_000017.10:g.43009797C>A , CM000679.1:g.43009797C>A	GRCh37
NC_000017.9:g.40365323C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000593135.6:c.1239-223G>T MANE Select	ENSP00000465992.1:n.1239-223G>T
ENST00000585687.1:n.474G>T
ENST00000587309.5:c.1239-187G>T	ENSP00000465377.1:n.1239-187G>T
ENST00000590129.1:c.1266-187G>T	ENSP00000465501.1:n.1266-187G>T
ENST00000593135.5:c.1239-223G>T	ENSP00000465992.1:n.1239-223G>T
NM_001264573.1:c.1239-187G>T	NP_001251503.1:n.1239-187G>T
NM_001265577.1:c.1239-223G>T	NP_001252506.1:n.1239-223G>T
XM_011524385.1:c.1266-187G>T	XP_011522687.1:n.1266-187G>T
XM_011524386.1:c.1239-187G>T	XP_011522688.1:n.1239-187G>T
XM_011524387.1:c.1266-187G>T	XP_011522689.1:n.1266-187G>T
XM_011524388.1:c.1266-223G>T	XP_011522690.1:n.1266-223G>T
XM_011524389.1:c.1266-187G>T	XP_011522691.1:n.1266-187G>T
XM_011524390.1:c.1161-187G>T	XP_011522692.1:n.1161-187G>T
XM_011524391.1:c.*79G>T	XP_011522693.1:n.*79G>T
XM_011524385.2:c.1266-187G>T	XP_011522687.1:n.1266-187G>T
XM_011524386.2:c.1239-187G>T	XP_011522688.1:n.1239-187G>T
XM_011524387.2:c.1266-187G>T	XP_011522689.1:n.1266-187G>T
XM_011524388.3:c.1266-223G>T	XP_011522690.1:n.1266-223G>T
XM_011524389.2:c.1266-187G>T	XP_011522691.1:n.1266-187G>T
XM_011524390.2:c.1161-187G>T	XP_011522692.1:n.1161-187G>T
XM_011524391.3:c.*79G>T	XP_011522693.1:n.*79G>T
NM_001264573.2:c.1239-187G>T	NP_001251503.1:n.1239-187G>T
NM_001265577.2:c.1239-223G>T MANE Select	NP_001252506.1:n.1239-223G>T