Canonical Allele Identifier: CA17858903

Gene: KIF1B

Linked Data

• dbSNP Id: rs940639374
• gnomAD v3: 1-10378638-G-C
• gnomAD v4: 1-10378638-G-C
• MyVariant Identifiers: chr1:g.10438696G>C (hg19) ; chr1:g.10378638G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10378638G>C , CM000663.2:g.10378638G>C	GRCh38
NC_000001.10:g.10438696G>C , CM000663.1:g.10438696G>C	GRCh37
NC_000001.9:g.10361283G>C	NCBI36
NG_008069.1:g.172933G>C , LRG_252:g.172933G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000676179.1:c.*2051G>C MANE Select	ENSP00000502065.1:n.*2051G>C
ENST00000377081.5:c.*236G>C	ENSP00000366284.1:n.*236G>C
ENST00000377086.5:c.*2051G>C	ENSP00000366290.1:n.*2051G>C
ENST00000620295.2:c.5666G>C	ENSP00000478500.1:n.5666G>C
ENST00000622724.3:c.5630G>C	ENSP00000480063.1:n.5630G>C
NM_015074.3:c.*2051G>C , LRG_252t1:c.*2051G>C	NP_055889.2:n.*2051G>C
NM_001365951.1:c.*2051G>C	NP_001352880.1:n.*2051G>C
NM_001365952.1:c.*2051G>C	NP_001352881.1:n.*2051G>C
NM_001365951.3:c.*2051G>C MANE Select	NP_001352880.1:n.*2051G>C