Canonical Allele Identifier: CA395931643

Gene: MMP2

Linked Data

• MyVariant Identifiers: chr16:g.55516966C>G (hg19) ; chr16:g.55483054C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.55483054C>G , CM000678.2:g.55483054C>G	GRCh38
NC_000016.9:g.55516966C>G , CM000678.1:g.55516966C>G	GRCh37
NC_000016.8:g.54074467C>G	NCBI36
NG_008989.1:g.8886C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219070.9:c.299C>G MANE Select	ENSP00000219070.4:p.Pro100Arg
ENST00000219070.8:c.299C>G	ENSP00000219070.4:p.Pro100Arg
ENST00000437642.6:c.149C>G	ENSP00000394237.2:p.Pro50Arg
ENST00000543485.5:c.71C>G	ENSP00000444143.1:p.Pro24Arg
ENST00000564864.5:c.71C>G	ENSP00000456096.1:p.Pro24Arg
ENST00000568715.5:c.71C>G	ENSP00000457949.1:p.Pro24Arg
ENST00000570308.5:c.71C>G	ENSP00000461421.1:p.Pro24Arg
NM_001127891.2:c.149C>G	NP_001121363.1:p.Pro50Arg
NM_001302508.1:c.71C>G	NP_001289437.1:p.Pro24Arg
NM_001302509.1:c.71C>G	NP_001289438.1:p.Pro24Arg
NM_001302510.1:c.71C>G	NP_001289439.1:p.Pro24Arg
NM_004530.5:c.299C>G	NP_004521.1:p.Pro100Arg
NM_004530.6:c.299C>G MANE Select	NP_004521.1:p.Pro100Arg
NM_001127891.3:c.149C>G	NP_001121363.1:p.Pro50Arg
NM_001302509.2:c.71C>G	NP_001289438.1:p.Pro24Arg
NM_001302510.2:c.71C>G	NP_001289439.1:p.Pro24Arg