Canonical Allele Identifier: CA510642058
Gene: MMP9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.44638598C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46009959C>T , CM000682.2:g.46009959C>T GRCh38
NC_000020.10:g.44638598C>T , CM000682.1:g.44638598C>T GRCh37
NC_000020.9:g.44072005C>T NCBI36
NG_011468.1:g.6052C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000372330.3:c.232C>T MANE Select ENSP00000361405.3:p.Leu78=
NM_004994.2:c.232C>T NP_004985.2:p.Leu78=
NM_004994.3:c.232C>T MANE Select NP_004985.2:p.Leu78=