Canonical Allele Identifier: CA382234759
Gene: MMP3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.102713427C>G (hg19) chr11:g.102842696C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102842696C>G , CM000673.2:g.102842696C>G GRCh38
NC_000011.9:g.102713427C>G , CM000673.1:g.102713427C>G GRCh37
NC_000011.8:g.102218637C>G NCBI36
NG_012100.1:g.5916G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000299855.10:c.326G>C MANE Select ENSP00000299855.5:p.Trp109Ser
ENST00000299855.9:c.326G>C ENSP00000299855.5:p.Trp109Ser
ENST00000524478.1:c.*168G>C ENSP00000435255.1:n.*168G>C
NM_002422.3:c.326G>C NP_002413.1:p.Trp109Ser
NM_002422.4:c.326G>C NP_002413.1:p.Trp109Ser
NM_002422.5:c.326G>C MANE Select NP_002413.1:p.Trp109Ser
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Search 100 bp 3'