Canonical Allele Identifier: CA13562873
Gene: MMP3 HGNC NCBI
gnomAD v2:
11:102713777 G / C
gnomAD v3:
11:102843046 G / C
gnomAD v4:
chr11-102843046-G-C
Joint Max Group AF 0.67264856 (EAS)
Genomes Max Group AF 0.67799651 (SAS)
Exomes Max Group AF 0.673071 (EAS)
ClinVar RCV:
RCV001667385
ClinVar Variation:
1262266
dbSNP:
678815
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102843046G>C , CM000673.2:g.102843046G>C GRCh38
NC_000011.9:g.102713777G>C , CM000673.1:g.102713777G>C GRCh37
NC_000011.8:g.102218987G>C NCBI36
NG_012100.1:g.5566C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000299855.10:c.106-130C>G MANE Select ENSP00000299855.5:n.106-130C>G
ENST00000299855.9:c.106-130C>G ENSP00000299855.5:n.106-130C>G
ENST00000524478.1:c.77-130C>G ENSP00000435255.1:n.77-130C>G
NM_002422.3:c.106-130C>G NP_002413.1:n.106-130C>G
NM_002422.4:c.106-130C>G NP_002413.1:n.106-130C>G
NM_002422.5:c.106-130C>G MANE Select NP_002413.1:n.106-130C>G
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