Canonical Allele Identifier: CA409214152
Gene: MMP9 HGNC NCBI

Linked Data

gnomAD v4: 20-46011312-C-A
MyVariant Identifiers: chr20:g.44639951C>A (hg19) chr20:g.46011312C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46011312C>A , CM000682.2:g.46011312C>A GRCh38
NC_000020.10:g.44639951C>A , CM000682.1:g.44639951C>A GRCh37
NC_000020.9:g.44073358C>A NCBI36
NG_011468.1:g.7405C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000372330.3:c.819C>A MANE Select ENSP00000361405.3:p.Ser273Arg
NM_004994.2:c.819C>A NP_004985.2:p.Ser273Arg
NM_004994.3:c.819C>A MANE Select NP_004985.2:p.Ser273Arg
Search 100 bp 5'
Search 100 bp 3'