Canonical Allele Identifier: CA382234773
Gene: MMP3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.102713434G>C (hg19) chr11:g.102842703G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102842703G>C , CM000673.2:g.102842703G>C GRCh38
NC_000011.9:g.102713434G>C , CM000673.1:g.102713434G>C GRCh37
NC_000011.8:g.102218644G>C NCBI36
NG_012100.1:g.5909C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000299855.10:c.319C>G MANE Select ENSP00000299855.5:p.Pro107Ala
ENST00000299855.9:c.319C>G ENSP00000299855.5:p.Pro107Ala
ENST00000524478.1:c.*161C>G ENSP00000435255.1:n.*161C>G
NM_002422.3:c.319C>G NP_002413.1:p.Pro107Ala
NM_002422.4:c.319C>G NP_002413.1:p.Pro107Ala
NM_002422.5:c.319C>G MANE Select NP_002413.1:p.Pro107Ala
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