Canonical Allele Identifier: CA382209572
Gene: MMP7 HGNC NCBI

Linked Data

dbSNP Id: rs1351136974
gnomAD v2: 11-102398511-C-A
gnomAD v4: 11-102527780-C-A
MyVariant Identifiers: chr11:g.102398511C>A (hg19) chr11:g.102527780C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102527780C>A , CM000673.2:g.102527780C>A GRCh38
NC_000011.9:g.102398511C>A , CM000673.1:g.102398511C>A GRCh37
NC_000011.8:g.101903721C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000260227.5:c.312G>T MANE Select ENSP00000260227.4:p.Trp104Cys
ENST00000260227.4:c.312G>T ENSP00000260227.4:p.Trp104Cys
ENST00000531200.1:n.359G>T
ENST00000533366.5:n.362G>T
NM_002423.3:c.312G>T NP_002414.1:p.Trp104Cys
NM_002423.4:c.312G>T NP_002414.1:p.Trp104Cys
NM_002423.5:c.312G>T MANE Select NP_002414.1:p.Trp104Cys
Search 100 bp 5'
Search 100 bp 3'