Canonical Allele Identifier: CA44383378
Gene: RAB10 HGNC NCBI

Linked Data

dbSNP Id: rs938772057
MyVariant Identifiers: chr2:g.26358244A>G (hg19) chr2:g.26135375A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26135375A>G , CM000664.2:g.26135375A>G GRCh38
NC_000002.11:g.26358244A>G , CM000664.1:g.26358244A>G GRCh37
NC_000002.10:g.26211748A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000264710.5:c.*354A>G MANE Select ENSP00000264710.4:n.*354A>G
ENST00000264710.4:c.*354A>G ENSP00000264710.4:n.*354A>G
NM_016131.4:c.*354A>G NP_057215.3:n.*354A>G
XM_024452565.1:c.*354A>G XP_024308333.1:n.*354A>G
NM_016131.5:c.*354A>G MANE Select NP_057215.3:n.*354A>G
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