Canonical Allele Identifier: CA409212936
Gene: MMP9 HGNC NCBI

Linked Data

dbSNP Id: rs2084274932
MyVariant Identifiers: chr20:g.44639612C>T (hg19) chr20:g.46010973C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46010973C>T , CM000682.2:g.46010973C>T GRCh38
NC_000020.10:g.44639612C>T , CM000682.1:g.44639612C>T GRCh37
NC_000020.9:g.44073019C>T NCBI36
NG_011468.1:g.7066C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000372330.3:c.572C>T MANE Select ENSP00000361405.3:p.Ala191Val
NM_004994.2:c.572C>T NP_004985.2:p.Ala191Val
NM_004994.3:c.572C>T MANE Select NP_004985.2:p.Ala191Val
Search 100 bp 5'
Search 100 bp 3'