Canonical Allele Identifier: CA733133950
Gene: TOMM20 HGNC NCBI

Linked Data

dbSNP Id: rs1330514100
gnomAD v3: 1-235112912-T-C
gnomAD v4: 1-235112912-T-C
MyVariant Identifiers: chr1:g.235276227T>C (hg19) chr1:g.235112912T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.235112912T>C , CM000663.2:g.235112912T>C GRCh38
NC_000001.10:g.235276227T>C , CM000663.1:g.235276227T>C GRCh37
NC_000001.9:g.233342850T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000366607.5:c.394-804A>G MANE Select ENSP00000355566.4:n.394-804A>G
ENST00000366607.4:c.394-804A>G ENSP00000355566.4:n.394-804A>G
ENST00000467767.5:n.294-804A>G
ENST00000473132.1:n.360-804A>G
NM_014765.2:c.394-804A>G NP_055580.1:n.394-804A>G
NM_014765.3:c.394-804A>G MANE Select NP_055580.1:n.394-804A>G
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