Canonical Allele Identifier: CA382234952
Gene: MMP3 HGNC NCBI

Linked Data

dbSNP Id: rs1859032092
gnomAD v3: 11-102842789-T-C
gnomAD v4: 11-102842789-T-C
MyVariant Identifiers: chr11:g.102713520T>C (hg19) chr11:g.102842789T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102842789T>C , CM000673.2:g.102842789T>C GRCh38
NC_000011.9:g.102713520T>C , CM000673.1:g.102713520T>C GRCh37
NC_000011.8:g.102218730T>C NCBI36
NG_012100.1:g.5823A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000299855.10:c.233A>G MANE Select ENSP00000299855.5:p.Lys78Arg
ENST00000299855.9:c.233A>G ENSP00000299855.5:p.Lys78Arg
ENST00000524478.1:c.*75A>G ENSP00000435255.1:n.*75A>G
NM_002422.3:c.233A>G NP_002413.1:p.Lys78Arg
NM_002422.4:c.233A>G NP_002413.1:p.Lys78Arg
NM_002422.5:c.233A>G MANE Select NP_002413.1:p.Lys78Arg
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Search 100 bp 3'