Canonical Allele Identifier: CA2574960071
Gene: MMP7 HGNC NCBI

Linked Data

dbSNP Id: rs1858688293

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102527677T>C , CM000673.2:g.102527677T>C GRCh38
NC_000011.9:g.102398408T>C , CM000673.1:g.102398408T>C GRCh37
NC_000011.8:g.101903618T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000260227.5:c.336-5A>G MANE Select ENSP00000260227.4:n.336-5A>G
ENST00000260227.4:c.336-5A>G ENSP00000260227.4:n.336-5A>G
ENST00000531200.1:n.383-5A>G
ENST00000533366.5:n.386-5A>G
NM_002423.3:c.336-5A>G NP_002414.1:n.336-5A>G
NM_002423.4:c.336-5A>G NP_002414.1:n.336-5A>G
NM_002423.5:c.336-5A>G MANE Select NP_002414.1:n.336-5A>G