Canonical Allele Identifier: CA913405420

Gene: TOMM20

Linked Data

• dbSNP Id: rs1558127604
• gnomAD v2: 1-235276239-T-C
• gnomAD v3: 1-235112924-T-C
• gnomAD v4: 1-235112924-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235112924T>C , CM000663.2:g.235112924T>C	GRCh38
NC_000001.10:g.235276239T>C , CM000663.1:g.235276239T>C	GRCh37
NC_000001.9:g.233342862T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000366607.5:c.394-816A>G MANE Select	ENSP00000355566.4:n.394-816A>G
ENST00000366607.4:c.394-816A>G	ENSP00000355566.4:n.394-816A>G
ENST00000467767.5:n.294-816A>G
ENST00000473132.1:n.360-816A>G
NM_014765.2:c.394-816A>G	NP_055580.1:n.394-816A>G
NM_014765.3:c.394-816A>G MANE Select	NP_055580.1:n.394-816A>G