Canonical Allele Identifier: CA744849029
Gene: MMP9 HGNC NCBI

Linked Data

dbSNP Id: rs1260716459
gnomAD v4: 20-46011513-T-C
MyVariant Identifiers: chr20:g.44640152T>C (hg19) chr20:g.46011513T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46011513T>C , CM000682.2:g.46011513T>C GRCh38
NC_000020.10:g.44640152T>C , CM000682.1:g.44640152T>C GRCh37
NC_000020.9:g.44073559T>C NCBI36
NG_011468.1:g.7606T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000372330.3:c.824-61T>C MANE Select ENSP00000361405.3:n.824-61T>C
NM_004994.2:c.824-61T>C NP_004985.2:n.824-61T>C
NM_004994.3:c.824-61T>C MANE Select NP_004985.2:n.824-61T>C
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