Canonical Allele Identifier: CA409214435
Gene: MMP9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.44640220C>G (hg19) chr20:g.46011581C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46011581C>G , CM000682.2:g.46011581C>G GRCh38
NC_000020.10:g.44640220C>G , CM000682.1:g.44640220C>G GRCh37
NC_000020.9:g.44073627C>G NCBI36
NG_011468.1:g.7674C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000372330.3:c.831C>G MANE Select ENSP00000361405.3:p.Tyr277Ter
NM_004994.2:c.831C>G NP_004985.2:p.Tyr277Ter
NM_004994.3:c.831C>G MANE Select NP_004985.2:p.Tyr277Ter
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