Canonical Allele Identifier: CA395931722

Gene: MMP2

Linked Data

• MyVariant Identifiers: chr16:g.55517004T>G (hg19) ; chr16:g.55483092T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.55483092T>G , CM000678.2:g.55483092T>G	GRCh38
NC_000016.9:g.55517004T>G , CM000678.1:g.55517004T>G	GRCh37
NC_000016.8:g.54074505T>G	NCBI36
NG_008989.1:g.8924T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219070.9:c.337T>G MANE Select	ENSP00000219070.4:p.Phe113Val
ENST00000219070.8:c.337T>G	ENSP00000219070.4:p.Phe113Val
ENST00000437642.6:c.187T>G	ENSP00000394237.2:p.Phe63Val
ENST00000543485.5:c.109T>G	ENSP00000444143.1:p.Phe37Val
ENST00000564864.5:c.109T>G	ENSP00000456096.1:p.Phe37Val
ENST00000568715.5:c.109T>G	ENSP00000457949.1:p.Phe37Val
ENST00000570308.5:c.109T>G	ENSP00000461421.1:p.Phe37Val
NM_001127891.2:c.187T>G	NP_001121363.1:p.Phe63Val
NM_001302508.1:c.109T>G	NP_001289437.1:p.Phe37Val
NM_001302509.1:c.109T>G	NP_001289438.1:p.Phe37Val
NM_001302510.1:c.109T>G	NP_001289439.1:p.Phe37Val
NM_004530.5:c.337T>G	NP_004521.1:p.Phe113Val
NM_004530.6:c.337T>G MANE Select	NP_004521.1:p.Phe113Val
NM_001127891.3:c.187T>G	NP_001121363.1:p.Phe63Val
NM_001302509.2:c.109T>G	NP_001289438.1:p.Phe37Val
NM_001302510.2:c.109T>G	NP_001289439.1:p.Phe37Val