Canonical Allele Identifier: CA409213030
Gene: MMP9 HGNC NCBI

Linked Data

dbSNP Id: rs2084275151
MyVariant Identifiers: chr20:g.44639656G>C (hg19) chr20:g.46011017G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46011017G>C , CM000682.2:g.46011017G>C GRCh38
NC_000020.10:g.44639656G>C , CM000682.1:g.44639656G>C GRCh37
NC_000020.9:g.44073063G>C NCBI36
NG_011468.1:g.7110G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000372330.3:c.616G>C MANE Select ENSP00000361405.3:p.Asp206His
NM_004994.2:c.616G>C NP_004985.2:p.Asp206His
NM_004994.3:c.616G>C MANE Select NP_004985.2:p.Asp206His
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