Canonical Allele Identifier: CA409215333
Gene: MMP9 HGNC NCBI

Linked Data

dbSNP Id: rs1600575329
MyVariant Identifiers: chr20:g.44640329T>G (hg19) chr20:g.46011690T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46011690T>G , CM000682.2:g.46011690T>G GRCh38
NC_000020.10:g.44640329T>G , CM000682.1:g.44640329T>G GRCh37
NC_000020.9:g.44073736T>G NCBI36
NG_011468.1:g.7783T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000372330.3:c.940T>G MANE Select ENSP00000361405.3:p.Cys314Gly
NM_004994.2:c.940T>G NP_004985.2:p.Cys314Gly
NM_004994.3:c.940T>G MANE Select NP_004985.2:p.Cys314Gly
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Search 100 bp 3'