Canonical Allele Identifier: CA382234940
Gene: MMP3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.102713514T>A (hg19) chr11:g.102842783T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102842783T>A , CM000673.2:g.102842783T>A GRCh38
NC_000011.9:g.102713514T>A , CM000673.1:g.102713514T>A GRCh37
NC_000011.8:g.102218724T>A NCBI36
NG_012100.1:g.5829A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000299855.10:c.239A>T MANE Select ENSP00000299855.5:p.Asp80Val
ENST00000299855.9:c.239A>T ENSP00000299855.5:p.Asp80Val
ENST00000524478.1:c.*81A>T ENSP00000435255.1:n.*81A>T
NM_002422.3:c.239A>T NP_002413.1:p.Asp80Val
NM_002422.4:c.239A>T NP_002413.1:p.Asp80Val
NM_002422.5:c.239A>T MANE Select NP_002413.1:p.Asp80Val
Search 100 bp 5'
Search 100 bp 3'