Canonical Allele Identifier: CA1228503024
Gene: TOMM20 HGNC NCBI

Linked Data

dbSNP Id: rs1660762301
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.235112906A>T , CM000663.2:g.235112906A>T GRCh38
NC_000001.10:g.235276221A>T , CM000663.1:g.235276221A>T GRCh37
NC_000001.9:g.233342844A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000366607.5:c.394-798T>A MANE Select ENSP00000355566.4:n.394-798T>A
ENST00000366607.4:c.394-798T>A ENSP00000355566.4:n.394-798T>A
ENST00000467767.5:n.294-798T>A
ENST00000473132.1:n.360-798T>A
NM_014765.2:c.394-798T>A NP_055580.1:n.394-798T>A
NM_014765.3:c.394-798T>A MANE Select NP_055580.1:n.394-798T>A
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