Canonical Allele Identifier: CA721882360
Gene: MMP2 HGNC NCBI

Linked Data

dbSNP Id: rs1220599308
MyVariant Identifiers: chr16:g.55508941T>C (hg19) chr16:g.55475029T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.55475029T>C , CM000678.2:g.55475029T>C GRCh38
NC_000016.9:g.55508941T>C , CM000678.1:g.55508941T>C GRCh37
NC_000016.8:g.54066442T>C NCBI36
NG_008989.1:g.861T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000570308.5:c.-75-7880T>C ENSP00000461421.1:n.-75-7880T>C
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