Canonical Allele Identifier: CA395931660

Gene: MMP2

Linked Data

• dbSNP Id: rs2142344678
• COSMIC: COSM3510283
• MyVariant Identifiers: chr16:g.55516975G>A (hg19) ; chr16:g.55483063G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.55483063G>A , CM000678.2:g.55483063G>A	GRCh38
NC_000016.9:g.55516975G>A , CM000678.1:g.55516975G>A	GRCh37
NC_000016.8:g.54074476G>A	NCBI36
NG_008989.1:g.8895G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219070.9:c.308G>A MANE Select	ENSP00000219070.4:p.Gly103Asp
ENST00000219070.8:c.308G>A	ENSP00000219070.4:p.Gly103Asp
ENST00000437642.6:c.158G>A	ENSP00000394237.2:p.Gly53Asp
ENST00000543485.5:c.80G>A	ENSP00000444143.1:p.Gly27Asp
ENST00000564864.5:c.80G>A	ENSP00000456096.1:p.Gly27Asp
ENST00000568715.5:c.80G>A	ENSP00000457949.1:p.Gly27Asp
ENST00000570308.5:c.80G>A	ENSP00000461421.1:p.Gly27Asp
NM_001127891.2:c.158G>A	NP_001121363.1:p.Gly53Asp
NM_001302508.1:c.80G>A	NP_001289437.1:p.Gly27Asp
NM_001302509.1:c.80G>A	NP_001289438.1:p.Gly27Asp
NM_001302510.1:c.80G>A	NP_001289439.1:p.Gly27Asp
NM_004530.5:c.308G>A	NP_004521.1:p.Gly103Asp
NM_004530.6:c.308G>A MANE Select	NP_004521.1:p.Gly103Asp
NM_001127891.3:c.158G>A	NP_001121363.1:p.Gly53Asp
NM_001302509.2:c.80G>A	NP_001289438.1:p.Gly27Asp
NM_001302510.2:c.80G>A	NP_001289439.1:p.Gly27Asp