Canonical Allele Identifier: CA382234992
Gene: MMP3 HGNC NCBI

Linked Data

dbSNP Id: rs1859032875
gnomAD v4: 11-102842808-C-T
MyVariant Identifiers: chr11:g.102713539C>T (hg19) chr11:g.102842808C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102842808C>T , CM000673.2:g.102842808C>T GRCh38
NC_000011.9:g.102713539C>T , CM000673.1:g.102713539C>T GRCh37
NC_000011.8:g.102218749C>T NCBI36
NG_012100.1:g.5804G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000299855.10:c.214G>A MANE Select ENSP00000299855.5:p.Gly72Arg
ENST00000299855.9:c.214G>A ENSP00000299855.5:p.Gly72Arg
ENST00000524478.1:c.*56G>A ENSP00000435255.1:n.*56G>A
NM_002422.3:c.214G>A NP_002413.1:p.Gly72Arg
NM_002422.4:c.214G>A NP_002413.1:p.Gly72Arg
NM_002422.5:c.214G>A MANE Select NP_002413.1:p.Gly72Arg
Search 100 bp 5'
Search 100 bp 3'