Canonical Allele Identifier: CA315635437
Gene: MMP9 HGNC NCBI

Linked Data

dbSNP Id: rs201549219
gnomAD v4: 20-46011720-A-T
MyVariant Identifiers: chr20:g.44640359A>T (hg19) chr20:g.46011720A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46011720A>T , CM000682.2:g.46011720A>T GRCh38
NC_000020.10:g.44640359A>T , CM000682.1:g.44640359A>T GRCh37
NC_000020.9:g.44073766A>T NCBI36
NG_011468.1:g.7813A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000372330.3:c.970A>T MANE Select ENSP00000361405.3:p.Lys324Ter
NM_004994.2:c.970A>T NP_004985.2:p.Lys324Ter
NM_004994.3:c.970A>T MANE Select NP_004985.2:p.Lys324Ter
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Search 100 bp 3'