Canonical Allele Identifier: CA767263153
Gene: RAB10 HGNC NCBI

Linked Data

dbSNP Id: rs1333273287
gnomAD v4: 2-26135240-A-G
MyVariant Identifiers: chr2:g.26358109A>G (hg19) chr2:g.26135240A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26135240A>G , CM000664.2:g.26135240A>G GRCh38
NC_000002.11:g.26358109A>G , CM000664.1:g.26358109A>G GRCh37
NC_000002.10:g.26211613A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000264710.5:c.*219A>G MANE Select ENSP00000264710.4:n.*219A>G
ENST00000264710.4:c.*219A>G ENSP00000264710.4:n.*219A>G
ENST00000495146.5:n.1185A>G
NM_016131.4:c.*219A>G NP_057215.3:n.*219A>G
XM_024452565.1:c.*219A>G XP_024308333.1:n.*219A>G
NM_016131.5:c.*219A>G MANE Select NP_057215.3:n.*219A>G
Search 100 bp 5'
Search 100 bp 3'