Canonical Allele Identifier: CA382234950
Gene: MMP3 HGNC NCBI

Linked Data

gnomAD v4: 11-102842788-C-G
MyVariant Identifiers: chr11:g.102713519C>G (hg19) chr11:g.102842788C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102842788C>G , CM000673.2:g.102842788C>G GRCh38
NC_000011.9:g.102713519C>G , CM000673.1:g.102713519C>G GRCh37
NC_000011.8:g.102218729C>G NCBI36
NG_012100.1:g.5824G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000299855.10:c.234G>C MANE Select ENSP00000299855.5:p.Lys78Asn
ENST00000299855.9:c.234G>C ENSP00000299855.5:p.Lys78Asn
ENST00000524478.1:c.*76G>C ENSP00000435255.1:n.*76G>C
NM_002422.3:c.234G>C NP_002413.1:p.Lys78Asn
NM_002422.4:c.234G>C NP_002413.1:p.Lys78Asn
NM_002422.5:c.234G>C MANE Select NP_002413.1:p.Lys78Asn
Search 100 bp 5'
Search 100 bp 3'