Canonical Allele Identifier: CA636176858
Gene: MMP9 HGNC NCBI

Linked Data

dbSNP Id: rs1243941699
gnomAD v2: 20-44640424-C-T
MyVariant Identifiers: chr20:g.44640424C>T (hg19) chr20:g.46011785C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46011785C>T , CM000682.2:g.46011785C>T GRCh38
NC_000020.10:g.44640424C>T , CM000682.1:g.44640424C>T GRCh37
NC_000020.9:g.44073831C>T NCBI36
NG_011468.1:g.7878C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000372330.3:c.997+38C>T MANE Select ENSP00000361405.3:n.997+38C>T
NM_004994.2:c.997+38C>T NP_004985.2:n.997+38C>T
NM_004994.3:c.997+38C>T MANE Select NP_004985.2:n.997+38C>T
Search 100 bp 5'
Search 100 bp 3'