Canonical Allele Identifier: CA155748619
Gene: TOMM7 HGNC NCBI

Linked Data

dbSNP Id: rs915167528
MyVariant Identifiers: chr7:g.22856459C>G (hg19) chr7:g.22816840C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22816840C>G , CM000669.2:g.22816840C>G GRCh38
NC_000007.13:g.22856459C>G , CM000669.1:g.22856459C>G GRCh37
NC_000007.12:g.22822984C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000358435.9:c.152+1160G>C MANE Select ENSP00000351214.4:n.152+1160G>C
ENST00000358435.8:c.152+1160G>C ENSP00000351214.4:n.152+1160G>C
ENST00000372879.8:c.289+572G>C ENSP00000361970.4:n.289+572G>C
ENST00000405021.7:c.140+1160G>C ENSP00000385203.3:n.140+1160G>C
ENST00000463284.2:n.174-3655G>C
ENST00000483581.1:n.336+1160G>C
NM_019059.3:c.152+1160G>C NP_061932.1:n.152+1160G>C
NM_019059.4:c.152+1160G>C NP_061932.1:n.152+1160G>C
NM_019059.5:c.152+1160G>C MANE Select NP_061932.1:n.152+1160G>C
NR_168014.1:n.178+1160G>C
NR_168015.1:n.130-3655G>C
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