Canonical Allele Identifier: CA12834235

Gene: KIF13B

Linked Data

• dbSNP Id: rs13251954
• gnomAD v2: 8-28995022-A-G
• gnomAD v3: 8-29137505-A-G
• gnomAD v4: 8-29137505-A-G
• MyVariant Identifiers: chr8:g.28995022A>G (hg19) ; chr8:g.29137505A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.29137505A>G , CM000670.2:g.29137505A>G	GRCh38
NC_000008.10:g.28995022A>G , CM000670.1:g.28995022A>G	GRCh37
NC_000008.9:g.29050941A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000524189.6:c.2613+2558T>C MANE Select	ENSP00000427900.1:n.2613+2558T>C
ENST00000524189.5:c.2613+2558T>C	ENSP00000427900.1:n.2613+2558T>C
NM_015254.3:c.2613+2558T>C	NP_056069.2:n.2613+2558T>C
XM_005273458.1:c.2613+2558T>C	XP_005273515.1:n.2613+2558T>C
XM_011544457.1:c.2613+2558T>C	XP_011542759.1:n.2613+2558T>C
XM_011544458.1:c.2613+2558T>C	XP_011542760.1:n.2613+2558T>C
XM_011544459.1:c.2421+2558T>C	XP_011542761.1:n.2421+2558T>C
XM_011544460.1:c.2421+2558T>C	XP_011542762.1:n.2421+2558T>C
XM_011544461.1:c.2421+2558T>C	XP_011542763.1:n.2421+2558T>C
XR_949621.1:n.93-1020A>G
XM_011544459.3:c.2421+2558T>C	XP_011542761.1:n.2421+2558T>C
XM_011544460.3:c.2421+2558T>C	XP_011542762.1:n.2421+2558T>C
XM_017013257.1:c.2613+2558T>C	XP_016868746.1:n.2613+2558T>C
NM_015254.4:c.2613+2558T>C MANE Select	NP_056069.2:n.2613+2558T>C