Canonical Allele Identifier: CA409211872
Gene: MMP9 HGNC NCBI

Linked Data

gnomAD v4: 20-46009948-T-C
MyVariant Identifiers: chr20:g.44638587T>C (hg19) chr20:g.46009948T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46009948T>C , CM000682.2:g.46009948T>C GRCh38
NC_000020.10:g.44638587T>C , CM000682.1:g.44638587T>C GRCh37
NC_000020.9:g.44071994T>C NCBI36
NG_011468.1:g.6041T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000372330.3:c.221T>C MANE Select ENSP00000361405.3:p.Leu74Pro
NM_004994.2:c.221T>C NP_004985.2:p.Leu74Pro
NM_004994.3:c.221T>C MANE Select NP_004985.2:p.Leu74Pro
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