Canonical Allele Identifier: CA382209649
Gene: MMP7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.102398519G>C (hg19) chr11:g.102527788G>C (hg38)
JSON-LD

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000260227.5:c.304C>G MANE Select ENSP00000260227.4:p.Pro102Ala
ENST00000260227.4:c.304C>G ENSP00000260227.4:p.Pro102Ala
ENST00000531200.1:n.351C>G
ENST00000533366.5:n.354C>G
NM_002423.3:c.304C>G NP_002414.1:p.Pro102Ala
NM_002423.4:c.304C>G NP_002414.1:p.Pro102Ala
NM_002423.5:c.304C>G MANE Select NP_002414.1:p.Pro102Ala
Search 100 bp 5'
Search 100 bp 3'