Canonical Allele Identifier: CA382234895
Gene: MMP3 HGNC NCBI

Linked Data

dbSNP Id: rs1555005783
gnomAD v2: 11-102713493-A-G
gnomAD v4: 11-102842762-A-G
MyVariant Identifiers: chr11:g.102713493A>G (hg19) chr11:g.102842762A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102842762A>G , CM000673.2:g.102842762A>G GRCh38
NC_000011.9:g.102713493A>G , CM000673.1:g.102713493A>G GRCh37
NC_000011.8:g.102218703A>G NCBI36
NG_012100.1:g.5850T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000299855.10:c.260T>C MANE Select ENSP00000299855.5:p.Met87Thr
ENST00000299855.9:c.260T>C ENSP00000299855.5:p.Met87Thr
ENST00000524478.1:c.*102T>C ENSP00000435255.1:n.*102T>C
NM_002422.3:c.260T>C NP_002413.1:p.Met87Thr
NM_002422.4:c.260T>C NP_002413.1:p.Met87Thr
NM_002422.5:c.260T>C MANE Select NP_002413.1:p.Met87Thr
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