Canonical Allele Identifier: CA44383265
Gene: RAB10 HGNC NCBI

Linked Data

dbSNP Id: rs899319754
gnomAD v2: 2-26358001-T-C
gnomAD v3: 2-26135132-T-C
gnomAD v4: 2-26135132-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26135132T>C , CM000664.2:g.26135132T>C GRCh38
NC_000002.11:g.26358001T>C , CM000664.1:g.26358001T>C GRCh37
NC_000002.10:g.26211505T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000264710.5:c.*111T>C MANE Select ENSP00000264710.4:n.*111T>C
ENST00000264710.4:c.*111T>C ENSP00000264710.4:n.*111T>C
ENST00000495146.5:n.1077T>C
NM_016131.4:c.*111T>C NP_057215.3:n.*111T>C
XM_024452565.1:c.*111T>C XP_024308333.1:n.*111T>C
NM_016131.5:c.*111T>C MANE Select NP_057215.3:n.*111T>C