Canonical Allele Identifier: CA884737392

Gene: KIF1B

Linked Data

• dbSNP Id: rs1384013798
• gnomAD v3: 1-10325342-C-A
• gnomAD v4: 1-10325342-C-A
• MyVariant Identifiers: chr1:g.10385400C>A (hg19) ; chr1:g.10325342C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10325342C>A , CM000663.2:g.10325342C>A	GRCh38
NC_000001.10:g.10385400C>A , CM000663.1:g.10385400C>A	GRCh37
NC_000001.9:g.10307987C>A	NCBI36
NG_008069.1:g.119637C>A , LRG_252:g.119637C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000696502.1:c.2537+447C>A	ENSP00000512668.1:n.2537+447C>A
ENST00000696503.1:c.2600+447C>A	ENSP00000512669.1:n.2600+447C>A
ENST00000696504.1:c.2600+447C>A	ENSP00000512670.1:n.2600+447C>A
ENST00000676179.1:c.2675+447C>A MANE Select	ENSP00000502065.1:n.2675+447C>A
ENST00000263934.10:c.2537+447C>A	ENSP00000263934.6:n.2537+447C>A
ENST00000377081.5:c.2675+447C>A	ENSP00000366284.1:n.2675+447C>A
ENST00000377086.5:c.2675+447C>A	ENSP00000366290.1:n.2675+447C>A
ENST00000620295.2:c.2633+447C>A	ENSP00000478500.1:n.2633+447C>A
ENST00000622724.3:c.2597+447C>A	ENSP00000480063.1:n.2597+447C>A
NM_015074.3:c.2537+447C>A , LRG_252t1:c.2537+447C>A	NP_055889.2:n.2537+447C>A
NM_001365951.1:c.2675+447C>A	NP_001352880.1:n.2675+447C>A
NM_001365952.1:c.2675+447C>A	NP_001352881.1:n.2675+447C>A
NM_001365951.3:c.2675+447C>A MANE Select	NP_001352880.1:n.2675+447C>A