Canonical Allele Identifier: CA44383383
Gene: RAB10 HGNC NCBI

Linked Data

dbSNP Id: rs547581073
gnomAD v3: 2-26135391-C-T
gnomAD v4: 2-26135391-C-T
MyVariant Identifiers: chr2:g.26358260C>T (hg19) chr2:g.26135391C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26135391C>T , CM000664.2:g.26135391C>T GRCh38
NC_000002.11:g.26358260C>T , CM000664.1:g.26358260C>T GRCh37
NC_000002.10:g.26211764C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000264710.5:c.*370C>T MANE Select ENSP00000264710.4:n.*370C>T
ENST00000264710.4:c.*370C>T ENSP00000264710.4:n.*370C>T
NM_016131.4:c.*370C>T NP_057215.3:n.*370C>T
XM_024452565.1:c.*370C>T XP_024308333.1:n.*370C>T
NM_016131.5:c.*370C>T MANE Select NP_057215.3:n.*370C>T
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