Canonical Allele Identifier: CA836784086
Gene: TOMM7 HGNC NCBI

Linked Data

dbSNP Id: rs1214648351
MyVariant Identifiers: chr7:g.22856488T>C (hg19) chr7:g.22816869T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22816869T>C , CM000669.2:g.22816869T>C GRCh38
NC_000007.13:g.22856488T>C , CM000669.1:g.22856488T>C GRCh37
NC_000007.12:g.22823013T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000358435.9:c.152+1131A>G MANE Select ENSP00000351214.4:n.152+1131A>G
ENST00000358435.8:c.152+1131A>G ENSP00000351214.4:n.152+1131A>G
ENST00000372879.8:c.289+543A>G ENSP00000361970.4:n.289+543A>G
ENST00000405021.7:c.140+1131A>G ENSP00000385203.3:n.140+1131A>G
ENST00000463284.2:n.174-3684A>G
ENST00000483581.1:n.336+1131A>G
NM_019059.3:c.152+1131A>G NP_061932.1:n.152+1131A>G
NM_019059.4:c.152+1131A>G NP_061932.1:n.152+1131A>G
NM_019059.5:c.152+1131A>G MANE Select NP_061932.1:n.152+1131A>G
NR_168014.1:n.178+1131A>G
NR_168015.1:n.130-3684A>G
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