Canonical Allele Identifier: CA409212244
Gene: MMP9 HGNC NCBI

Linked Data

gnomAD v4: 20-46010061-G-T
MyVariant Identifiers: chr20:g.44638700G>T (hg19) chr20:g.46010061G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46010061G>T , CM000682.2:g.46010061G>T GRCh38
NC_000020.10:g.44638700G>T , CM000682.1:g.44638700G>T GRCh37
NC_000020.9:g.44072107G>T NCBI36
NG_011468.1:g.6154G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000372330.3:c.334G>T MANE Select ENSP00000361405.3:p.Gly112Cys
NM_004994.2:c.334G>T NP_004985.2:p.Gly112Cys
NM_004994.3:c.334G>T MANE Select NP_004985.2:p.Gly112Cys
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