Canonical Allele Identifier: CA601669340

Gene: MMP7

Linked Data

• dbSNP Id: rs1477391887
• gnomAD v2: 11-102398406-A-G
• gnomAD v3: 11-102527675-A-G
• gnomAD v4: 11-102527675-A-G
• MyVariant Identifiers: chr11:g.102398406A>G (hg19) ; chr11:g.102527675A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.102527675A>G , CM000673.2:g.102527675A>G	GRCh38
NC_000011.9:g.102398406A>G , CM000673.1:g.102398406A>G	GRCh37
NC_000011.8:g.101903616A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260227.5:c.336-3T>C MANE Select	ENSP00000260227.4:n.336-3T>C
ENST00000260227.4:c.336-3T>C	ENSP00000260227.4:n.336-3T>C
ENST00000531200.1:n.383-3T>C
ENST00000533366.5:n.386-3T>C
NM_002423.3:c.336-3T>C	NP_002414.1:n.336-3T>C
NM_002423.4:c.336-3T>C	NP_002414.1:n.336-3T>C
NM_002423.5:c.336-3T>C MANE Select	NP_002414.1:n.336-3T>C