Canonical Allele Identifier: CA751790454
Gene: MMP11 HGNC NCBI

Linked Data

dbSNP Id: rs1381340160
gnomAD v4: 22-23771269-C-T
MyVariant Identifiers: chr22:g.24113456C>T (hg19) chr22:g.23771269C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23771269C>T , CM000684.2:g.23771269C>T GRCh38
NC_000022.10:g.24113456C>T , CM000684.1:g.24113456C>T GRCh37
NC_000022.9:g.22443456C>T NCBI36
NG_029443.1:g.3421C>T
NG_034223.1:g.1704G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000465385.5:n.720C>T
ENST00000477567.5:n.234C>T
ENST00000489582.5:n.134+2476C>T
XR_001755453.1:n.720C>T
XR_001755454.1:n.720C>T
Search 100 bp 5'
Search 100 bp 3'