Canonical Allele Identifier: CA2563489773

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102789835A>T , CM000673.2:g.102789835A>T GRCh38
NC_000011.9:g.102660566A>T , CM000673.1:g.102660566A>T GRCh37
NC_000011.8:g.102165776A>T NCBI36
NG_011740.1:g.13401T>A
NG_011740.2:g.13401T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000680179.1:n.1165T>A (MMP1)
ENST00000681445.1:n.1161T>A (MMP1)
ENST00000681643.1:n.1187T>A (MMP1)
ENST00000371455.7:n.325-8189A>T (WTAPP1)
ENST00000525739.6:n.390-3310A>T (WTAPP1)
ENST00000544704.1:n.344+5771A>T (WTAPP1)
NR_038390.1:n.390-3310A>T (WTAPP1)