Canonical Allele Identifier: CA2223710355
Gene: MMP2 HGNC NCBI

Linked Data

dbSNP Id: rs1567372722

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.55482873G>A , CM000678.2:g.55482873G>A GRCh38
NC_000016.9:g.55516785G>A , CM000678.1:g.55516785G>A GRCh37
NC_000016.8:g.54074286G>A NCBI36
NG_008989.1:g.8705G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000219070.9:c.154-36G>A MANE Select ENSP00000219070.4:n.154-36G>A
ENST00000219070.8:c.154-36G>A ENSP00000219070.4:n.154-36G>A
ENST00000437642.6:c.4-36G>A ENSP00000394237.2:n.4-36G>A
ENST00000543485.5:c.-75-36G>A ENSP00000444143.1:n.-75-36G>A
ENST00000564864.5:c.-75-36G>A ENSP00000456096.1:n.-75-36G>A
ENST00000568715.5:c.-75-36G>A ENSP00000457949.1:n.-75-36G>A
ENST00000570308.5:c.-75-36G>A ENSP00000461421.1:n.-75-36G>A
NM_001127891.2:c.4-36G>A NP_001121363.1:n.4-36G>A
NM_001302508.1:c.-75-36G>A NP_001289437.1:n.-75-36G>A
NM_001302509.1:c.-75-36G>A NP_001289438.1:n.-75-36G>A
NM_001302510.1:c.-75-36G>A NP_001289439.1:n.-75-36G>A
NM_004530.5:c.154-36G>A NP_004521.1:n.154-36G>A
NM_004530.6:c.154-36G>A MANE Select NP_004521.1:n.154-36G>A
NM_001127891.3:c.4-36G>A NP_001121363.1:n.4-36G>A
NM_001302509.2:c.-75-36G>A NP_001289438.1:n.-75-36G>A
NM_001302510.2:c.-75-36G>A NP_001289439.1:n.-75-36G>A