Canonical Allele Identifier: CA382234739
Gene: MMP3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.102713419T>A (hg19) chr11:g.102842688T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102842688T>A , CM000673.2:g.102842688T>A GRCh38
NC_000011.9:g.102713419T>A , CM000673.1:g.102713419T>A GRCh37
NC_000011.8:g.102218629T>A NCBI36
NG_012100.1:g.5924A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000299855.10:c.334A>T MANE Select ENSP00000299855.5:p.Thr112Ser
ENST00000299855.9:c.334A>T ENSP00000299855.5:p.Thr112Ser
ENST00000524478.1:c.*176A>T ENSP00000435255.1:n.*176A>T
NM_002422.3:c.334A>T NP_002413.1:p.Thr112Ser
NM_002422.4:c.334A>T NP_002413.1:p.Thr112Ser
NM_002422.5:c.334A>T MANE Select NP_002413.1:p.Thr112Ser
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