Canonical Allele Identifier: CA2633277177

Gene: MMP2

Linked Data

• gnomAD v4: 16-55482871-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.55482871A>G , CM000678.2:g.55482871A>G	GRCh38
NC_000016.9:g.55516783A>G , CM000678.1:g.55516783A>G	GRCh37
NC_000016.8:g.54074284A>G	NCBI36
NG_008989.1:g.8703A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000219070.9:c.154-38A>G MANE Select	ENSP00000219070.4:n.154-38A>G
ENST00000219070.8:c.154-38A>G	ENSP00000219070.4:n.154-38A>G
ENST00000437642.6:c.4-38A>G	ENSP00000394237.2:n.4-38A>G
ENST00000543485.5:c.-75-38A>G	ENSP00000444143.1:n.-75-38A>G
ENST00000564864.5:c.-75-38A>G	ENSP00000456096.1:n.-75-38A>G
ENST00000568715.5:c.-75-38A>G	ENSP00000457949.1:n.-75-38A>G
ENST00000570308.5:c.-75-38A>G	ENSP00000461421.1:n.-75-38A>G
NM_001127891.2:c.4-38A>G	NP_001121363.1:n.4-38A>G
NM_001302508.1:c.-75-38A>G	NP_001289437.1:n.-75-38A>G
NM_001302509.1:c.-75-38A>G	NP_001289438.1:n.-75-38A>G
NM_001302510.1:c.-75-38A>G	NP_001289439.1:n.-75-38A>G
NM_004530.5:c.154-38A>G	NP_004521.1:n.154-38A>G
NM_004530.6:c.154-38A>G MANE Select	NP_004521.1:n.154-38A>G
NM_001127891.3:c.4-38A>G	NP_001121363.1:n.4-38A>G
NM_001302509.2:c.-75-38A>G	NP_001289438.1:n.-75-38A>G
NM_001302510.2:c.-75-38A>G	NP_001289439.1:n.-75-38A>G