Canonical Allele Identifier: CA476738216
Gene: MMP3 HGNC NCBI

Linked Data

gnomAD v4: 11-102842680-A-G
MyVariant Identifiers: chr11:g.102713411A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102842680A>G , CM000673.2:g.102842680A>G GRCh38
NC_000011.9:g.102713411A>G , CM000673.1:g.102713411A>G GRCh37
NC_000011.8:g.102218621A>G NCBI36
NG_012100.1:g.5932T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000299855.10:c.342T>C MANE Select ENSP00000299855.5:p.Leu114=
ENST00000299855.9:c.342T>C ENSP00000299855.5:p.Leu114=
ENST00000524478.1:c.*184T>C ENSP00000435255.1:n.*184T>C
NM_002422.3:c.342T>C NP_002413.1:p.Leu114=
NM_002422.4:c.342T>C NP_002413.1:p.Leu114=
NM_002422.5:c.342T>C MANE Select NP_002413.1:p.Leu114=
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