Canonical Allele Identifier: CA1559085

Gene: RAB10

Linked Data

• dbSNP Id: rs761137629
• ExAC: 2:26357914 C / G
• gnomAD v2: 2-26357914-C-G
• gnomAD v3: 2-26135045-C-G
• gnomAD v4: 2-26135045-C-G
• MyVariant Identifiers: chr2:g.26357914C>G (hg19) ; chr2:g.26135045C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26135045C>G , CM000664.2:g.26135045C>G	GRCh38
NC_000002.11:g.26357914C>G , CM000664.1:g.26357914C>G	GRCh37
NC_000002.10:g.26211418C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264710.5:c.*24C>G MANE Select	ENSP00000264710.4:n.*24C>G
ENST00000264710.4:c.*24C>G	ENSP00000264710.4:n.*24C>G
ENST00000473035.1:n.548C>G
ENST00000495146.5:n.990C>G
NM_016131.4:c.*24C>G	NP_057215.3:n.*24C>G
XM_024452565.1:c.*24C>G	XP_024308333.1:n.*24C>G
NM_016131.5:c.*24C>G MANE Select	NP_057215.3:n.*24C>G