Canonical Allele Identifier: CA315635062
Gene: MMP9 HGNC NCBI

Linked Data

dbSNP Id: rs914407056
gnomAD v4: 20-46011122-C-T
MyVariant Identifiers: chr20:g.44639761C>T (hg19) chr20:g.46011122C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46011122C>T , CM000682.2:g.46011122C>T GRCh38
NC_000020.10:g.44639761C>T , CM000682.1:g.44639761C>T GRCh37
NC_000020.9:g.44073168C>T NCBI36
NG_011468.1:g.7215C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000372330.3:c.650-21C>T MANE Select ENSP00000361405.3:n.650-21C>T
NM_004994.2:c.650-21C>T NP_004985.2:n.650-21C>T
NM_004994.3:c.650-21C>T MANE Select NP_004985.2:n.650-21C>T
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