Canonical Allele Identifier: CA2615724366

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102789871G>T , CM000673.2:g.102789871G>T GRCh38
NC_000011.9:g.102660602G>T , CM000673.1:g.102660602G>T GRCh37
NC_000011.8:g.102165812G>T NCBI36
NG_011740.1:g.13365C>A
NG_011740.2:g.13365C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000680179.1:n.1129C>A (MMP1)
ENST00000681445.1:n.1125C>A (MMP1)
ENST00000681643.1:n.1151C>A (MMP1)
ENST00000371455.7:n.325-8153G>T (WTAPP1)
ENST00000525739.6:n.390-3274G>T (WTAPP1)
ENST00000544704.1:n.344+5807G>T (WTAPP1)
NR_038390.1:n.390-3274G>T (WTAPP1)