Canonical Allele Identifier: CA6247978
Gene: MMP7 HGNC NCBI

Linked Data

dbSNP Id: rs759831546

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102527866A>T , CM000673.2:g.102527866A>T GRCh38
NC_000011.9:g.102398597A>T , CM000673.1:g.102398597A>T GRCh37
NC_000011.8:g.101903807A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000260227.5:c.226T>A MANE Select ENSP00000260227.4:p.Ser76Thr
ENST00000260227.4:c.226T>A ENSP00000260227.4:p.Ser76Thr
ENST00000531200.1:n.273T>A
ENST00000533366.5:n.276T>A
NM_002423.3:c.226T>A NP_002414.1:p.Ser76Thr
NM_002423.4:c.226T>A NP_002414.1:p.Ser76Thr
NM_002423.5:c.226T>A MANE Select NP_002414.1:p.Ser76Thr