Canonical Allele Identifier: CA2615724345

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102789809C>A , CM000673.2:g.102789809C>A GRCh38
NC_000011.9:g.102660540C>A , CM000673.1:g.102660540C>A GRCh37
NC_000011.8:g.102165750C>A NCBI36
NG_011740.1:g.13427G>T
NG_011740.2:g.13427G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000680179.1:n.1191G>T (MMP1)
ENST00000681445.1:n.1187G>T (MMP1)
ENST00000681643.1:n.1213G>T (MMP1)
ENST00000371455.7:n.325-8215C>A (WTAPP1)
ENST00000525739.6:n.390-3336C>A (WTAPP1)
ENST00000544704.1:n.344+5745C>A (WTAPP1)
NR_038390.1:n.390-3336C>A (WTAPP1)