Canonical Allele Identifier: CA1013528926
Gene: TOMM20 HGNC NCBI

Linked Data

dbSNP Id: rs1660761850

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.235112881T>G , CM000663.2:g.235112881T>G GRCh38
NC_000001.10:g.235276196T>G , CM000663.1:g.235276196T>G GRCh37
NC_000001.9:g.233342819T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000366607.5:c.394-773A>C MANE Select ENSP00000355566.4:n.394-773A>C
ENST00000366607.4:c.394-773A>C ENSP00000355566.4:n.394-773A>C
ENST00000467767.5:n.294-773A>C
ENST00000473132.1:n.360-773A>C
NM_014765.2:c.394-773A>C NP_055580.1:n.394-773A>C
NM_014765.3:c.394-773A>C MANE Select NP_055580.1:n.394-773A>C