Canonical Allele Identifier: CA733133952
Gene: TOMM20 HGNC NCBI

Linked Data

dbSNP Id: rs1222089551
gnomAD v3: 1-235112919-A-T
gnomAD v4: 1-235112919-A-T
MyVariant Identifiers: chr1:g.235276234A>T (hg19) chr1:g.235112919A>T (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000366607.5:c.394-811T>A MANE Select ENSP00000355566.4:n.394-811T>A
ENST00000366607.4:c.394-811T>A ENSP00000355566.4:n.394-811T>A
ENST00000467767.5:n.294-811T>A
ENST00000473132.1:n.360-811T>A
NM_014765.2:c.394-811T>A NP_055580.1:n.394-811T>A
NM_014765.3:c.394-811T>A MANE Select NP_055580.1:n.394-811T>A
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