Canonical Allele Identifier: CA227359817
Gene: MMP1 HGNC NCBI
WTAPP1 HGNC NCBI

Linked Data

dbSNP Id: rs927705680
MyVariant Identifiers: chr11:g.102660484T>C (hg19) chr11:g.102789753T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102789753T>C , CM000673.2:g.102789753T>C GRCh38
NC_000011.9:g.102660484T>C , CM000673.1:g.102660484T>C GRCh37
NC_000011.8:g.102165694T>C NCBI36
NG_011740.1:g.13483A>G
NG_011740.2:g.13483A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000680179.1:n.1247A>G (MMP1)
ENST00000681445.1:n.1243A>G (MMP1)
ENST00000681643.1:n.1269A>G (MMP1)
ENST00000371455.7:n.325-8271T>C (WTAPP1)
ENST00000525739.6:n.390-3392T>C (WTAPP1)
ENST00000544704.1:n.344+5689T>C (WTAPP1)
NR_038390.1:n.390-3392T>C (WTAPP1)
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