Canonical Allele Identifier: CA8060043
Gene: MMP2 HGNC NCBI

Linked Data

dbSNP Id: rs752059182

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.55483072A>G , CM000678.2:g.55483072A>G GRCh38
NC_000016.9:g.55516984A>G , CM000678.1:g.55516984A>G GRCh37
NC_000016.8:g.54074485A>G NCBI36
NG_008989.1:g.8904A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000219070.9:c.317A>G MANE Select ENSP00000219070.4:p.Asp106Gly
ENST00000219070.8:c.317A>G ENSP00000219070.4:p.Asp106Gly
ENST00000437642.6:c.167A>G ENSP00000394237.2:p.Asp56Gly
ENST00000543485.5:c.89A>G ENSP00000444143.1:p.Asp30Gly
ENST00000564864.5:c.89A>G ENSP00000456096.1:p.Asp30Gly
ENST00000568715.5:c.89A>G ENSP00000457949.1:p.Asp30Gly
ENST00000570308.5:c.89A>G ENSP00000461421.1:p.Asp30Gly
NM_001127891.2:c.167A>G NP_001121363.1:p.Asp56Gly
NM_001302508.1:c.89A>G NP_001289437.1:p.Asp30Gly
NM_001302509.1:c.89A>G NP_001289438.1:p.Asp30Gly
NM_001302510.1:c.89A>G NP_001289439.1:p.Asp30Gly
NM_004530.5:c.317A>G NP_004521.1:p.Asp106Gly
NM_004530.6:c.317A>G MANE Select NP_004521.1:p.Asp106Gly
NM_001127891.3:c.167A>G NP_001121363.1:p.Asp56Gly
NM_001302509.2:c.89A>G NP_001289438.1:p.Asp30Gly
NM_001302510.2:c.89A>G NP_001289439.1:p.Asp30Gly