Canonical Allele Identifier: CA2261621290

Gene: KIF18B

Linked Data

• dbSNP Id: rs736866

Genomic Alleles

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

Transcript Alleles

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