Canonical Allele Identifier: CA2580600661

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102789676G= , CM000673.2:g.102789676G= GRCh38
NC_000011.9:g.102660407G= , CM000673.1:g.102660407G= GRCh37
NC_000011.8:g.102165617G= NCBI36
NG_011740.1:g.13560C=
NG_011740.2:g.13560C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000680179.1:n.1324C= (MMP1)
ENST00000681445.1:n.1320C= (MMP1)
ENST00000681643.1:n.1346C= (MMP1)
ENST00000371455.7:n.325-8348G= (WTAPP1)
ENST00000525739.6:n.390-3469G= (WTAPP1)
ENST00000544704.1:n.344+5612G= (WTAPP1)
NR_038390.1:n.390-3469G= (WTAPP1)