Canonical Allele Identifier: CA1028595243
Gene: RAB10 HGNC NCBI

Linked Data

dbSNP Id: rs1668082527
gnomAD v3: 2-26135117-T-C
gnomAD v4: 2-26135117-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26135117T>C , CM000664.2:g.26135117T>C GRCh38
NC_000002.11:g.26357986T>C , CM000664.1:g.26357986T>C GRCh37
NC_000002.10:g.26211490T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000264710.5:c.*96T>C MANE Select ENSP00000264710.4:n.*96T>C
ENST00000264710.4:c.*96T>C ENSP00000264710.4:n.*96T>C
ENST00000495146.5:n.1062T>C
NM_016131.4:c.*96T>C NP_057215.3:n.*96T>C
XM_024452565.1:c.*96T>C XP_024308333.1:n.*96T>C
NM_016131.5:c.*96T>C MANE Select NP_057215.3:n.*96T>C
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