Canonical Allele Identifier: CA281408299
Gene: MMP2 HGNC NCBI

Linked Data

dbSNP Id: rs1002040452
MyVariant Identifiers: chr16:g.55509078C>T (hg19) chr16:g.55475166C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.55475166C>T , CM000678.2:g.55475166C>T GRCh38
NC_000016.9:g.55509078C>T , CM000678.1:g.55509078C>T GRCh37
NC_000016.8:g.54066579C>T NCBI36
NG_008989.1:g.998C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000570308.5:c.-75-7743C>T ENSP00000461421.1:n.-75-7743C>T
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