Canonical Allele Identifier: CA476736570
Gene: MMP7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.102398544T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102527813T>C , CM000673.2:g.102527813T>C GRCh38
NC_000011.9:g.102398544T>C , CM000673.1:g.102398544T>C GRCh37
NC_000011.8:g.101903754T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000260227.5:c.279A>G MANE Select ENSP00000260227.4:p.Ala93=
ENST00000260227.4:c.279A>G ENSP00000260227.4:p.Ala93=
ENST00000531200.1:n.326A>G
ENST00000533366.5:n.329A>G
NM_002423.3:c.279A>G NP_002414.1:p.Ala93=
NM_002423.4:c.279A>G NP_002414.1:p.Ala93=
NM_002423.5:c.279A>G MANE Select NP_002414.1:p.Ala93=
Search 100 bp 5'
Search 100 bp 3'