Canonical Allele Identifier: CA721882412
Gene: MMP2 HGNC NCBI

Linked Data

dbSNP Id: rs1172598735
gnomAD v3: 16-55475080-T-C
gnomAD v4: 16-55475080-T-C
MyVariant Identifiers: chr16:g.55508992T>C (hg19) chr16:g.55475080T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.55475080T>C , CM000678.2:g.55475080T>C GRCh38
NC_000016.9:g.55508992T>C , CM000678.1:g.55508992T>C GRCh37
NC_000016.8:g.54066493T>C NCBI36
NG_008989.1:g.912T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000570308.5:c.-75-7829T>C ENSP00000461421.1:n.-75-7829T>C
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