Canonical Allele Identifier: CA670917431
Gene: MMP3 HGNC NCBI

Linked Data

dbSNP Id: rs1390462231
MyVariant Identifiers: chr11:g.102842607T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102842607T>C , CM000673.2:g.102842607T>C GRCh38
NC_000011.9:g.102713338T>C , CM000673.1:g.102713338T>C GRCh37
NC_000011.8:g.102218548T>C NCBI36
NG_012100.1:g.6005A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000299855.10:c.351-28A>G MANE Select ENSP00000299855.5:n.351-28A>G
ENST00000299855.9:c.351-28A>G ENSP00000299855.5:n.351-28A>G
ENST00000524478.1:c.*193-28A>G ENSP00000435255.1:n.*193-28A>G
NM_002422.3:c.351-28A>G NP_002413.1:n.351-28A>G
NM_002422.4:c.351-28A>G NP_002413.1:n.351-28A>G
NM_002422.5:c.351-28A>G MANE Select NP_002413.1:n.351-28A>G