Canonical Allele Identifier: CA281397602

Gene: MMP2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.55486666C>G , CM000678.2:g.55486666C>G	GRCh38
NC_000016.9:g.55520578C>G , CM000678.1:g.55520578C>G	GRCh37
NC_000016.8:g.54078079C>G	NCBI36
NG_008989.1:g.12498C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219070.9:c.832+889C>G MANE Select	ENSP00000219070.4:n.832+889C>G
ENST00000219070.8:c.832+889C>G	ENSP00000219070.4:n.832+889C>G
ENST00000437642.6:c.682+889C>G	ENSP00000394237.2:n.682+889C>G
ENST00000543485.5:c.604+889C>G	ENSP00000444143.1:n.604+889C>G
ENST00000570308.5:c.604+889C>G	ENSP00000461421.1:n.604+889C>G
NM_001127891.2:c.682+889C>G	NP_001121363.1:n.682+889C>G
NM_001302508.1:c.604+889C>G	NP_001289437.1:n.604+889C>G
NM_001302509.1:c.604+889C>G	NP_001289438.1:n.604+889C>G
NM_001302510.1:c.604+889C>G	NP_001289439.1:n.604+889C>G
NM_004530.5:c.832+889C>G	NP_004521.1:n.832+889C>G
NM_004530.6:c.832+889C>G MANE Select	NP_004521.1:n.832+889C>G
NM_001127891.3:c.682+889C>G	NP_001121363.1:n.682+889C>G
NM_001302509.2:c.604+889C>G	NP_001289438.1:n.604+889C>G
NM_001302510.2:c.604+889C>G	NP_001289439.1:n.604+889C>G