Canonical Allele Identifier: CA15165173
Gene: RAB10 HGNC NCBI

Linked Data

dbSNP Id: rs142787485
gnomAD v2: 2-26358156-A-G
gnomAD v3: 2-26135287-A-G
gnomAD v4: 2-26135287-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26135287A>G , CM000664.2:g.26135287A>G GRCh38
NC_000002.11:g.26358156A>G , CM000664.1:g.26358156A>G GRCh37
NC_000002.10:g.26211660A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000264710.5:c.*266A>G MANE Select ENSP00000264710.4:n.*266A>G
ENST00000264710.4:c.*266A>G ENSP00000264710.4:n.*266A>G
ENST00000495146.5:n.1232A>G
NM_016131.4:c.*266A>G NP_057215.3:n.*266A>G
XM_024452565.1:c.*266A>G XP_024308333.1:n.*266A>G
NM_016131.5:c.*266A>G MANE Select NP_057215.3:n.*266A>G