Canonical Allele Identifier: CA1228503032
Gene: TOMM20 HGNC NCBI

Linked Data

dbSNP Id: rs764246212

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.235112926G>A , CM000663.2:g.235112926G>A GRCh38
NC_000001.10:g.235276241G>A , CM000663.1:g.235276241G>A GRCh37
NC_000001.9:g.233342864G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000366607.5:c.394-818C>T MANE Select ENSP00000355566.4:n.394-818C>T
ENST00000366607.4:c.394-818C>T ENSP00000355566.4:n.394-818C>T
ENST00000467767.5:n.294-818C>T
ENST00000473132.1:n.360-818C>T
NM_014765.2:c.394-818C>T NP_055580.1:n.394-818C>T
NM_014765.3:c.394-818C>T MANE Select NP_055580.1:n.394-818C>T