Canonical Allele Identifier: CA227293269
Gene: MMP7 HGNC NCBI

Linked Data

dbSNP Id: rs757811267
MyVariant Identifiers: chr11:g.102398586T>G (hg19) chr11:g.102527855T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102527855T>G , CM000673.2:g.102527855T>G GRCh38
NC_000011.9:g.102398586T>G , CM000673.1:g.102398586T>G GRCh37
NC_000011.8:g.101903796T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000260227.5:c.237A>C MANE Select ENSP00000260227.4:p.Ile79=
ENST00000260227.4:c.237A>C ENSP00000260227.4:p.Ile79=
ENST00000531200.1:n.284A>C
ENST00000533366.5:n.287A>C
NM_002423.3:c.237A>C NP_002414.1:p.Ile79=
NM_002423.4:c.237A>C NP_002414.1:p.Ile79=
NM_002423.5:c.237A>C MANE Select NP_002414.1:p.Ile79=
Search 100 bp 5'
Search 100 bp 3'