Canonical Allele Identifier: CA10607294
Gene: KIF1B HGNC NCBI

Linked Data

ClinVar Variation Id: 291618
ClinVar RCV Id: RCV000264101
dbSNP Id: rs1536262
gnomAD v2: 1-10438687-C-T
gnomAD v3: 1-10378629-C-T
gnomAD v4: 1-10378629-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.10378629C>T , CM000663.2:g.10378629C>T GRCh38
NC_000001.10:g.10438687C>T , CM000663.1:g.10438687C>T GRCh37
NC_000001.9:g.10361274C>T NCBI36
NG_008069.1:g.172924C>T , LRG_252:g.172924C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000676179.1:c.*2042C>T MANE Select ENSP00000502065.1:n.*2042C>T
ENST00000377081.5:c.*227C>T ENSP00000366284.1:n.*227C>T
ENST00000377086.5:c.*2042C>T ENSP00000366290.1:n.*2042C>T
ENST00000620295.2:c.5657C>T ENSP00000478500.1:n.5657C>T
ENST00000622724.3:c.5621C>T ENSP00000480063.1:n.5621C>T
NM_015074.3:c.*2042C>T , LRG_252t1:c.*2042C>T NP_055889.2:n.*2042C>T
NM_001365951.1:c.*2042C>T NP_001352880.1:n.*2042C>T
NM_001365952.1:c.*2042C>T NP_001352881.1:n.*2042C>T
NM_001365951.3:c.*2042C>T MANE Select NP_001352880.1:n.*2042C>T