Canonical Allele Identifier: CA395931782

Gene: MMP2

Linked Data

• MyVariant Identifiers: chr16:g.55517031A>C (hg19) ; chr16:g.55483119A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.55483119A>C , CM000678.2:g.55483119A>C	GRCh38
NC_000016.9:g.55517031A>C , CM000678.1:g.55517031A>C	GRCh37
NC_000016.8:g.54074532A>C	NCBI36
NG_008989.1:g.8951A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219070.9:c.364A>C MANE Select	ENSP00000219070.4:p.Asn122His
ENST00000219070.8:c.364A>C	ENSP00000219070.4:p.Asn122His
ENST00000437642.6:c.214A>C	ENSP00000394237.2:p.Asn72His
ENST00000543485.5:c.136A>C	ENSP00000444143.1:p.Asn46His
ENST00000564864.5:c.136A>C	ENSP00000456096.1:p.Asn46His
ENST00000568715.5:c.136A>C	ENSP00000457949.1:p.Asn46His
ENST00000570308.5:c.136A>C	ENSP00000461421.1:p.Asn46His
NM_001127891.2:c.214A>C	NP_001121363.1:p.Asn72His
NM_001302508.1:c.136A>C	NP_001289437.1:p.Asn46His
NM_001302509.1:c.136A>C	NP_001289438.1:p.Asn46His
NM_001302510.1:c.136A>C	NP_001289439.1:p.Asn46His
NM_004530.5:c.364A>C	NP_004521.1:p.Asn122His
NM_004530.6:c.364A>C MANE Select	NP_004521.1:p.Asn122His
NM_001127891.3:c.214A>C	NP_001121363.1:p.Asn72His
NM_001302509.2:c.136A>C	NP_001289438.1:p.Asn46His
NM_001302510.2:c.136A>C	NP_001289439.1:p.Asn46His