Canonical Allele Identifier: CA415881686

Gene: KIF1B

Linked Data

• gnomAD v4: 1-10324845-T-C
• MyVariant Identifiers: chr1:g.10384903T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10324845T>C , CM000663.2:g.10324845T>C	GRCh38
NC_000001.10:g.10384903T>C , CM000663.1:g.10384903T>C	GRCh37
NC_000001.9:g.10307490T>C	NCBI36
NG_008069.1:g.119140T>C , LRG_252:g.119140T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696502.1:c.2487T>C	ENSP00000512668.1:p.Thr829=
ENST00000696503.1:c.2550T>C	ENSP00000512669.1:p.Thr850=
ENST00000696504.1:c.2550T>C	ENSP00000512670.1:p.Thr850=
ENST00000676179.1:c.2625T>C MANE Select	ENSP00000502065.1:p.Thr875=
ENST00000263934.10:c.2487T>C	ENSP00000263934.6:p.Thr829=
ENST00000377081.5:c.2625T>C	ENSP00000366284.1:p.Thr875=
ENST00000377086.5:c.2625T>C	ENSP00000366290.1:p.Thr875=
ENST00000620295.2:c.2583T>C	ENSP00000478500.1:p.Thr861=
ENST00000622724.3:c.2547T>C	ENSP00000480063.1:p.Thr849=
NM_015074.3:c.2487T>C , LRG_252t1:c.2487T>C	NP_055889.2:p.Thr829=
NM_001365951.1:c.2625T>C	NP_001352880.1:p.Thr875=
NM_001365952.1:c.2625T>C	NP_001352881.1:p.Thr875=
NM_001365951.3:c.2625T>C MANE Select	NP_001352880.1:p.Thr875=