Canonical Allele Identifier: CA531389196
Gene: RAB10 HGNC NCBI

Linked Data

dbSNP Id: rs1354975485
gnomAD v2: 2-26358106-G-T
gnomAD v3: 2-26135237-G-T
gnomAD v4: 2-26135237-G-T
MyVariant Identifiers: chr2:g.26358106G>T (hg19) chr2:g.26135237G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26135237G>T , CM000664.2:g.26135237G>T GRCh38
NC_000002.11:g.26358106G>T , CM000664.1:g.26358106G>T GRCh37
NC_000002.10:g.26211610G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000264710.5:c.*216G>T MANE Select ENSP00000264710.4:n.*216G>T
ENST00000264710.4:c.*216G>T ENSP00000264710.4:n.*216G>T
ENST00000495146.5:n.1182G>T
NM_016131.4:c.*216G>T NP_057215.3:n.*216G>T
XM_024452565.1:c.*216G>T XP_024308333.1:n.*216G>T
NM_016131.5:c.*216G>T MANE Select NP_057215.3:n.*216G>T
Search 100 bp 5'
Search 100 bp 3'