Canonical Allele Identifier: CA2580600665

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102789833C= , CM000673.2:g.102789833C= GRCh38
NC_000011.9:g.102660564C= , CM000673.1:g.102660564C= GRCh37
NC_000011.8:g.102165774C= NCBI36
NG_011740.1:g.13403G=
NG_011740.2:g.13403G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000680179.1:n.1167G= (MMP1)
ENST00000681445.1:n.1163G= (MMP1)
ENST00000681643.1:n.1189G= (MMP1)
ENST00000371455.7:n.325-8191C= (WTAPP1)
ENST00000525739.6:n.390-3312C= (WTAPP1)
ENST00000544704.1:n.344+5769C= (WTAPP1)
NR_038390.1:n.390-3312C= (WTAPP1)