Canonical Allele Identifier: CA338342422
Gene: KIF1B HGNC NCBI

Linked Data

dbSNP Id: rs1287254475
gnomAD v2: 1-10405953-A-G
gnomAD v3: 1-10345895-A-G
gnomAD v4: 1-10345895-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.10345895A>G , CM000663.2:g.10345895A>G GRCh38
NC_000001.10:g.10405953A>G , CM000663.1:g.10405953A>G GRCh37
NC_000001.9:g.10328540A>G NCBI36
NG_008069.1:g.140190A>G , LRG_252:g.140190A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696502.1:c.3802A>G ENSP00000512668.1:p.Met1268Val
ENST00000696503.1:c.3664A>G ENSP00000512669.1:p.Met1222Val
ENST00000696504.1:c.3664A>G ENSP00000512670.1:p.Met1222Val
ENST00000676179.1:c.3739A>G MANE Select ENSP00000502065.1:p.Met1247Val
ENST00000263934.10:c.3601A>G ENSP00000263934.6:p.Met1201Val
ENST00000377081.5:c.3739A>G ENSP00000366284.1:p.Met1247Val
ENST00000377086.5:c.3739A>G ENSP00000366290.1:p.Met1247Val
ENST00000465635.5:n.194A>G
ENST00000483340.1:n.275A>G
ENST00000620295.2:c.3697A>G ENSP00000478500.1:p.Met1233Val
ENST00000622724.3:c.3661A>G ENSP00000480063.1:p.Met1221Val
NM_015074.3:c.3601A>G , LRG_252t1:c.3601A>G NP_055889.2:p.Met1201Val
NM_001365951.1:c.3739A>G NP_001352880.1:p.Met1247Val
NM_001365952.1:c.3739A>G NP_001352881.1:p.Met1247Val
NM_001365951.3:c.3739A>G MANE Select NP_001352880.1:p.Met1247Val