Canonical Allele Identifier: CA6247959

Gene: MMP7

Linked Data

• dbSNP Id: rs766781129
• ExAC: 11:102398517 T / C
• gnomAD v2: 11-102398517-T-C
• gnomAD v4: 11-102527786-T-C
• MyVariant Identifiers: chr11:g.102398517T>C (hg19) ; chr11:g.102527786T>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000260227.5:c.306A>G MANE Select	ENSP00000260227.4:p.Pro102=
ENST00000260227.4:c.306A>G	ENSP00000260227.4:p.Pro102=
ENST00000531200.1:n.353A>G
ENST00000533366.5:n.356A>G
NM_002423.3:c.306A>G	NP_002414.1:p.Pro102=
NM_002423.4:c.306A>G	NP_002414.1:p.Pro102=
NM_002423.5:c.306A>G MANE Select	NP_002414.1:p.Pro102=