Canonical Allele Identifier: CA315634697
Gene: MMP9 HGNC NCBI

Linked Data

dbSNP Id: rs968015134
gnomAD v4: 20-46010778-G-A
MyVariant Identifiers: chr20:g.44639417G>A (hg19) chr20:g.46010778G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46010778G>A , CM000682.2:g.46010778G>A GRCh38
NC_000020.10:g.44639417G>A , CM000682.1:g.44639417G>A GRCh37
NC_000020.9:g.44072824G>A NCBI36
NG_011468.1:g.6871G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000372330.3:c.521-144G>A MANE Select ENSP00000361405.3:n.521-144G>A
NM_004994.2:c.521-144G>A NP_004985.2:n.521-144G>A
NM_004994.3:c.521-144G>A MANE Select NP_004985.2:n.521-144G>A
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