Canonical Allele Identifier: CA884737384

Gene: KIF1B

Linked Data

• dbSNP Id: rs1169204590
• gnomAD v3: 1-10325329-C-G
• gnomAD v4: 1-10325329-C-G
• MyVariant Identifiers: chr1:g.10385387C>G (hg19) ; chr1:g.10325329C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10325329C>G , CM000663.2:g.10325329C>G	GRCh38
NC_000001.10:g.10385387C>G , CM000663.1:g.10385387C>G	GRCh37
NC_000001.9:g.10307974C>G	NCBI36
NG_008069.1:g.119624C>G , LRG_252:g.119624C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000696502.1:c.2537+434C>G	ENSP00000512668.1:n.2537+434C>G
ENST00000696503.1:c.2600+434C>G	ENSP00000512669.1:n.2600+434C>G
ENST00000696504.1:c.2600+434C>G	ENSP00000512670.1:n.2600+434C>G
ENST00000676179.1:c.2675+434C>G MANE Select	ENSP00000502065.1:n.2675+434C>G
ENST00000263934.10:c.2537+434C>G	ENSP00000263934.6:n.2537+434C>G
ENST00000377081.5:c.2675+434C>G	ENSP00000366284.1:n.2675+434C>G
ENST00000377086.5:c.2675+434C>G	ENSP00000366290.1:n.2675+434C>G
ENST00000620295.2:c.2633+434C>G	ENSP00000478500.1:n.2633+434C>G
ENST00000622724.3:c.2597+434C>G	ENSP00000480063.1:n.2597+434C>G
NM_015074.3:c.2537+434C>G , LRG_252t1:c.2537+434C>G	NP_055889.2:n.2537+434C>G
NM_001365951.1:c.2675+434C>G	NP_001352880.1:n.2675+434C>G
NM_001365952.1:c.2675+434C>G	NP_001352881.1:n.2675+434C>G
NM_001365951.3:c.2675+434C>G MANE Select	NP_001352880.1:n.2675+434C>G