Canonical Allele Identifier: CA10647745
Community Standard Title: NM_004530.6(MMP2):c.*872C>T
Gene: MMP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.55506314C>T , CM000678.2:g.55506314C>T GRCh38
NC_000016.9:g.55540226C>T , CM000678.1:g.55540226C>T GRCh37
NC_000016.8:g.54097727C>T NCBI36
NG_008989.1:g.32146C>T

Transcript Alleles

HGVS Amino-acid Change
NM_004530.6:c.*872C>T MANE Select NP_004521.1:n.*872C>T
ENST00000219070.9:c.*872C>T MANE Select ENSP00000219070.4:n.*872C>T
NM_001127891.2:c.*872C>T NP_001121363.1:n.*872C>T
NM_001127891.3:c.*872C>T NP_001121363.1:n.*872C>T
NM_001302508.1:c.*872C>T NP_001289437.1:n.*872C>T
NM_001302509.1:c.*872C>T NP_001289438.1:n.*872C>T
NM_001302509.2:c.*872C>T NP_001289438.1:n.*872C>T
NM_001302510.1:c.*872C>T NP_001289439.1:n.*872C>T
NM_001302510.2:c.*872C>T NP_001289439.1:n.*872C>T
NM_004530.5:c.*872C>T NP_004521.1:n.*872C>T
ENST00000219070.8:c.*872C>T ENSP00000219070.4:n.*872C>T