Canonical Allele Identifier: CA1013528942
Gene: TOMM20 HGNC NCBI

Linked Data

dbSNP Id: rs1660762138

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.235112891T>C , CM000663.2:g.235112891T>C GRCh38
NC_000001.10:g.235276206T>C , CM000663.1:g.235276206T>C GRCh37
NC_000001.9:g.233342829T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000366607.5:c.394-783A>G MANE Select ENSP00000355566.4:n.394-783A>G
ENST00000366607.4:c.394-783A>G ENSP00000355566.4:n.394-783A>G
ENST00000467767.5:n.294-783A>G
ENST00000473132.1:n.360-783A>G
NM_014765.2:c.394-783A>G NP_055580.1:n.394-783A>G
NM_014765.3:c.394-783A>G MANE Select NP_055580.1:n.394-783A>G