Canonical Allele Identifier: CA155748618

Gene: TOMM7

Linked Data

• dbSNP Id: rs1035919495
• gnomAD v2: 7-22856458-T-G
• MyVariant Identifiers: chr7:g.22856458T>G (hg19) ; chr7:g.22816839T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.22816839T>G , CM000669.2:g.22816839T>G	GRCh38
NC_000007.13:g.22856458T>G , CM000669.1:g.22856458T>G	GRCh37
NC_000007.12:g.22822983T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358435.9:c.152+1161A>C MANE Select	ENSP00000351214.4:n.152+1161A>C
ENST00000358435.8:c.152+1161A>C	ENSP00000351214.4:n.152+1161A>C
ENST00000372879.8:c.289+573A>C	ENSP00000361970.4:n.289+573A>C
ENST00000405021.7:c.140+1161A>C	ENSP00000385203.3:n.140+1161A>C
ENST00000463284.2:n.174-3654A>C
ENST00000483581.1:n.336+1161A>C
NM_019059.3:c.152+1161A>C	NP_061932.1:n.152+1161A>C
NM_019059.4:c.152+1161A>C	NP_061932.1:n.152+1161A>C
NM_019059.5:c.152+1161A>C MANE Select	NP_061932.1:n.152+1161A>C
NR_168014.1:n.178+1161A>C
NR_168015.1:n.130-3654A>C