Canonical Allele Identifier: CA227344813
Gene: MMP3 HGNC NCBI
dbSNP:
3025066
gnomAD v2:
11:102710483 T / C
gnomAD v3:
11:102839752 T / C
gnomAD v4:
chr11-102839752-T-C
Joint Max Group AF 0.06901005 (NFE)
Genomes Max Group AF 0.06901005 (NFE)
MyVariant.info:
GRCh38 chr11:g.102839752T>C
GRCh37 chr11:g.102710483T>C
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102839752T>C , CM000673.2:g.102839752T>C GRCh38
NC_000011.9:g.102710483T>C , CM000673.1:g.102710483T>C GRCh37
NC_000011.8:g.102215693T>C NCBI36
NG_012100.1:g.8860A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000299855.10:c.935+356A>G MANE Select ENSP00000299855.5:n.935+356A>G
ENST00000299855.9:c.935+356A>G ENSP00000299855.5:n.935+356A>G
NM_002422.3:c.935+356A>G NP_002413.1:n.935+356A>G
NM_002422.4:c.935+356A>G NP_002413.1:n.935+356A>G
NM_002422.5:c.935+356A>G MANE Select NP_002413.1:n.935+356A>G
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