Canonical Allele Identifier: CA510751666
Gene: MMP9 HGNC NCBI

Linked Data

dbSNP Id: rs1459997671
MyVariant Identifiers: chr20:g.44639602C>T (hg19) chr20:g.46010963C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46010963C>T , CM000682.2:g.46010963C>T GRCh38
NC_000020.10:g.44639602C>T , CM000682.1:g.44639602C>T GRCh37
NC_000020.9:g.44073009C>T NCBI36
NG_011468.1:g.7056C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000372330.3:c.562C>T MANE Select ENSP00000361405.3:p.Leu188=
NM_004994.2:c.562C>T NP_004985.2:p.Leu188=
NM_004994.3:c.562C>T MANE Select NP_004985.2:p.Leu188=
Search 100 bp 5'
Search 100 bp 3'