Canonical Allele Identifier: CA2724632342

Linked Data

dbSNP Id: rs1591075586

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102789671T>A , CM000673.2:g.102789671T>A GRCh38
NC_000011.9:g.102660402T>A , CM000673.1:g.102660402T>A GRCh37
NC_000011.8:g.102165612T>A NCBI36
NG_011740.1:g.13565A>T
NG_011740.2:g.13565A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000680179.1:n.1329A>T (MMP1)
ENST00000681445.1:n.1325A>T (MMP1)
ENST00000681643.1:n.1351A>T (MMP1)
ENST00000371455.7:n.325-8353T>A (WTAPP1)
ENST00000525739.6:n.390-3474T>A (WTAPP1)
ENST00000544704.1:n.344+5607T>A (WTAPP1)
NR_038390.1:n.390-3474T>A (WTAPP1)