Canonical Allele Identifier: CA382234876
Gene: MMP3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.102713484G>T (hg19) chr11:g.102842753G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102842753G>T , CM000673.2:g.102842753G>T GRCh38
NC_000011.9:g.102713484G>T , CM000673.1:g.102713484G>T GRCh37
NC_000011.8:g.102218694G>T NCBI36
NG_012100.1:g.5859C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000299855.10:c.269C>A MANE Select ENSP00000299855.5:p.Pro90His
ENST00000299855.9:c.269C>A ENSP00000299855.5:p.Pro90His
ENST00000524478.1:c.*111C>A ENSP00000435255.1:n.*111C>A
NM_002422.3:c.269C>A NP_002413.1:p.Pro90His
NM_002422.4:c.269C>A NP_002413.1:p.Pro90His
NM_002422.5:c.269C>A MANE Select NP_002413.1:p.Pro90His
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