Canonical Allele Identifier: CA767263136
Gene: RAB10 HGNC NCBI

Linked Data

dbSNP Id: rs1212438557
gnomAD v3: 2-26135201-T-C
gnomAD v4: 2-26135201-T-C
MyVariant Identifiers: chr2:g.26358070T>C (hg19) chr2:g.26135201T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26135201T>C , CM000664.2:g.26135201T>C GRCh38
NC_000002.11:g.26358070T>C , CM000664.1:g.26358070T>C GRCh37
NC_000002.10:g.26211574T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000264710.5:c.*180T>C MANE Select ENSP00000264710.4:n.*180T>C
ENST00000264710.4:c.*180T>C ENSP00000264710.4:n.*180T>C
ENST00000495146.5:n.1146T>C
NM_016131.4:c.*180T>C NP_057215.3:n.*180T>C
XM_024452565.1:c.*180T>C XP_024308333.1:n.*180T>C
NM_016131.5:c.*180T>C MANE Select NP_057215.3:n.*180T>C
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