Canonical Allele Identifier: CA2602012899

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102789740A>C , CM000673.2:g.102789740A>C GRCh38
NC_000011.9:g.102660471A>C , CM000673.1:g.102660471A>C GRCh37
NC_000011.8:g.102165681A>C NCBI36
NG_011740.1:g.13496T>G
NG_011740.2:g.13496T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000680179.1:n.1260T>G (MMP1)
ENST00000681445.1:n.1256T>G (MMP1)
ENST00000681643.1:n.1282T>G (MMP1)
ENST00000371455.7:n.325-8284A>C (WTAPP1)
ENST00000525739.6:n.390-3405A>C (WTAPP1)
ENST00000544704.1:n.344+5676A>C (WTAPP1)
NR_038390.1:n.390-3405A>C (WTAPP1)