Canonical Allele Identifier: CA6247957
Gene: MMP7 HGNC NCBI

Linked Data

dbSNP Id: rs773457001
ExAC: 11:102398512 C / T
gnomAD v2: 11-102398512-C-T
gnomAD v4: 11-102527781-C-T
COSMIC: COSM3442676
MyVariant Identifiers: chr11:g.102398512C>T (hg19) chr11:g.102527781C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102527781C>T , CM000673.2:g.102527781C>T GRCh38
NC_000011.9:g.102398512C>T , CM000673.1:g.102398512C>T GRCh37
NC_000011.8:g.101903722C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000260227.5:c.311G>A MANE Select ENSP00000260227.4:p.Trp104Ter
ENST00000260227.4:c.311G>A ENSP00000260227.4:p.Trp104Ter
ENST00000531200.1:n.358G>A
ENST00000533366.5:n.361G>A
NM_002423.3:c.311G>A NP_002414.1:p.Trp104Ter
NM_002423.4:c.311G>A NP_002414.1:p.Trp104Ter
NM_002423.5:c.311G>A MANE Select NP_002414.1:p.Trp104Ter
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