Canonical Allele Identifier: CA227359706
Gene: MMP1 HGNC NCBI
WTAPP1 HGNC NCBI

Linked Data

dbSNP Id: rs768031544
MyVariant Identifiers: chr11:g.102660396A>G (hg19) chr11:g.102789665A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102789665A>G , CM000673.2:g.102789665A>G GRCh38
NC_000011.9:g.102660396A>G , CM000673.1:g.102660396A>G GRCh37
NC_000011.8:g.102165606A>G NCBI36
NG_011740.1:g.13571T>C
NG_011740.2:g.13571T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000680179.1:n.1335T>C (MMP1)
ENST00000681445.1:n.1331T>C (MMP1)
ENST00000681643.1:n.1357T>C (MMP1)
ENST00000371455.7:n.325-8359A>G (WTAPP1)
ENST00000525739.6:n.390-3480A>G (WTAPP1)
ENST00000544704.1:n.344+5601A>G (WTAPP1)
NR_038390.1:n.390-3480A>G (WTAPP1)
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