Canonical Allele Identifier: CA767263217
Gene: RAB10 HGNC NCBI

Linked Data

dbSNP Id: rs1382969622
gnomAD v4: 2-26135320-A-C
MyVariant Identifiers: chr2:g.26358189A>C (hg19) chr2:g.26135320A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26135320A>C , CM000664.2:g.26135320A>C GRCh38
NC_000002.11:g.26358189A>C , CM000664.1:g.26358189A>C GRCh37
NC_000002.10:g.26211693A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000264710.5:c.*299A>C MANE Select ENSP00000264710.4:n.*299A>C
ENST00000264710.4:c.*299A>C ENSP00000264710.4:n.*299A>C
ENST00000495146.5:n.1265A>C
NM_016131.4:c.*299A>C NP_057215.3:n.*299A>C
XM_024452565.1:c.*299A>C XP_024308333.1:n.*299A>C
NM_016131.5:c.*299A>C MANE Select NP_057215.3:n.*299A>C
Search 100 bp 5'
Search 100 bp 3'