Canonical Allele Identifier: CA382234933
Gene: MMP3 HGNC NCBI

Linked Data

dbSNP Id: rs1859031935
gnomAD v3: 11-102842780-G-T
gnomAD v4: 11-102842780-G-T
MyVariant Identifiers: chr11:g.102713511G>T (hg19) chr11:g.102842780G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102842780G>T , CM000673.2:g.102842780G>T GRCh38
NC_000011.9:g.102713511G>T , CM000673.1:g.102713511G>T GRCh37
NC_000011.8:g.102218721G>T NCBI36
NG_012100.1:g.5832C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000299855.10:c.242C>A MANE Select ENSP00000299855.5:p.Ser81Tyr
ENST00000299855.9:c.242C>A ENSP00000299855.5:p.Ser81Tyr
ENST00000524478.1:c.*84C>A ENSP00000435255.1:n.*84C>A
NM_002422.3:c.242C>A NP_002413.1:p.Ser81Tyr
NM_002422.4:c.242C>A NP_002413.1:p.Ser81Tyr
NM_002422.5:c.242C>A MANE Select NP_002413.1:p.Ser81Tyr
Search 100 bp 5'
Search 100 bp 3'