Canonical Allele Identifier: CA622283696
Gene: MMP2 HGNC NCBI

Linked Data

dbSNP Id: rs1359272440
gnomAD v2: 16-55509928-G-C
gnomAD v3: 16-55476016-G-C
gnomAD v4: 16-55476016-G-C
MyVariant Identifiers: chr16:g.55509928G>C (hg19) chr16:g.55476016G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.55476016G>C , CM000678.2:g.55476016G>C GRCh38
NC_000016.9:g.55509928G>C , CM000678.1:g.55509928G>C GRCh37
NC_000016.8:g.54067429G>C NCBI36
NG_008989.1:g.1848G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000570308.5:c.-75-6893G>C ENSP00000461421.1:n.-75-6893G>C
Search 100 bp 5'
Search 100 bp 3'