Canonical Allele Identifier: CA521138825

Gene: KIF1B

Linked Data

• dbSNP Id: rs1161720260
• gnomAD v2: 1-10428357-G-C
• gnomAD v3: 1-10368299-G-C
• gnomAD v4: 1-10368299-G-C
• MyVariant Identifiers: chr1:g.10428357G>C (hg19) ; chr1:g.10368299G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10368299G>C , CM000663.2:g.10368299G>C	GRCh38
NC_000001.10:g.10428357G>C , CM000663.1:g.10428357G>C	GRCh37
NC_000001.9:g.10350944G>C	NCBI36
NG_008069.1:g.162594G>C , LRG_252:g.162594G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696502.1:c.4816-168G>C	ENSP00000512668.1:n.4816-168G>C
ENST00000696503.1:c.4678-168G>C	ENSP00000512669.1:n.4678-168G>C
ENST00000696504.1:c.4678-168G>C	ENSP00000512670.1:n.4678-168G>C
ENST00000676179.1:c.4753-168G>C MANE Select	ENSP00000502065.1:n.4753-168G>C
ENST00000263934.10:c.4615-168G>C	ENSP00000263934.6:n.4615-168G>C
ENST00000377081.5:c.4753-168G>C	ENSP00000366284.1:n.4753-168G>C
ENST00000377086.5:c.4753-168G>C	ENSP00000366290.1:n.4753-168G>C
ENST00000470616.1:n.484-168G>C
ENST00000620295.2:c.4711-168G>C	ENSP00000478500.1:n.4711-168G>C
ENST00000622724.3:c.4675-168G>C	ENSP00000480063.1:n.4675-168G>C
ENST00000635499.1:c.798-168G>C
NM_015074.3:c.4615-168G>C , LRG_252t1:c.4615-168G>C	NP_055889.2:n.4615-168G>C
NM_001365951.1:c.4753-168G>C	NP_001352880.1:n.4753-168G>C
NM_001365952.1:c.4753-168G>C	NP_001352881.1:n.4753-168G>C
NM_001365951.3:c.4753-168G>C MANE Select	NP_001352880.1:n.4753-168G>C