Canonical Allele Identifier: CA476736538
Gene: MMP7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.102398517T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102527786T>G , CM000673.2:g.102527786T>G GRCh38
NC_000011.9:g.102398517T>G , CM000673.1:g.102398517T>G GRCh37
NC_000011.8:g.101903727T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000260227.5:c.306A>C MANE Select ENSP00000260227.4:p.Pro102=
ENST00000260227.4:c.306A>C ENSP00000260227.4:p.Pro102=
ENST00000531200.1:n.353A>C
ENST00000533366.5:n.356A>C
NM_002423.3:c.306A>C NP_002414.1:p.Pro102=
NM_002423.4:c.306A>C NP_002414.1:p.Pro102=
NM_002423.5:c.306A>C MANE Select NP_002414.1:p.Pro102=
Search 100 bp 5'
Search 100 bp 3'