Canonical Allele Identifier: CA1228503030
Gene: TOMM20 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.235112919A= , CM000663.2:g.235112919A= GRCh38
NC_000001.10:g.235276234A= , CM000663.1:g.235276234A= GRCh37
NC_000001.9:g.233342857A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000366607.5:c.394-811T= MANE Select ENSP00000355566.4:n.394-811T=
ENST00000366607.4:c.394-811T= ENSP00000355566.4:n.394-811T=
ENST00000467767.5:n.294-811T=
ENST00000473132.1:n.360-811T=
NM_014765.2:c.394-811T= NP_055580.1:n.394-811T=
NM_014765.3:c.394-811T= MANE Select NP_055580.1:n.394-811T=
Search 100 bp 5'
Search 100 bp 3'