Canonical Allele Identifier: CA127080
Gene: MMP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 17109
dbSNP Id: rs121912954

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.55485677C>A , CM000678.2:g.55485677C>A GRCh38
NC_000016.9:g.55519589C>A , CM000678.1:g.55519589C>A GRCh37
NC_000016.8:g.54077090C>A NCBI36
NG_008989.1:g.11509C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000219070.9:c.732C>A MANE Select ENSP00000219070.4:p.Tyr244Ter
ENST00000219070.8:c.732C>A ENSP00000219070.4:p.Tyr244Ter
ENST00000437642.6:c.582C>A ENSP00000394237.2:p.Tyr194Ter
ENST00000543485.5:c.504C>A ENSP00000444143.1:p.Tyr168Ter
ENST00000564864.5:c.504C>A ENSP00000456096.1:p.Tyr168Ter
ENST00000570308.5:c.504C>A ENSP00000461421.1:p.Tyr168Ter
NM_001127891.2:c.582C>A NP_001121363.1:p.Tyr194Ter
NM_001302508.1:c.504C>A NP_001289437.1:p.Tyr168Ter
NM_001302509.1:c.504C>A NP_001289438.1:p.Tyr168Ter
NM_001302510.1:c.504C>A NP_001289439.1:p.Tyr168Ter
NM_004530.5:c.732C>A NP_004521.1:p.Tyr244Ter
NM_004530.6:c.732C>A MANE Select NP_004521.1:p.Tyr244Ter
NM_001127891.3:c.582C>A NP_001121363.1:p.Tyr194Ter
NM_001302509.2:c.504C>A NP_001289438.1:p.Tyr168Ter
NM_001302510.2:c.504C>A NP_001289439.1:p.Tyr168Ter