Canonical Allele Identifier: CA382209633
Gene: MMP7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.102398519G>T (hg19) chr11:g.102527788G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102527788G>T , CM000673.2:g.102527788G>T GRCh38
NC_000011.9:g.102398519G>T , CM000673.1:g.102398519G>T GRCh37
NC_000011.8:g.101903729G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000260227.5:c.304C>A MANE Select ENSP00000260227.4:p.Pro102Thr
ENST00000260227.4:c.304C>A ENSP00000260227.4:p.Pro102Thr
ENST00000531200.1:n.351C>A
ENST00000533366.5:n.354C>A
NM_002423.3:c.304C>A NP_002414.1:p.Pro102Thr
NM_002423.4:c.304C>A NP_002414.1:p.Pro102Thr
NM_002423.5:c.304C>A MANE Select NP_002414.1:p.Pro102Thr
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