Canonical Allele Identifier: CA2724601850

Linked Data

dbSNP Id: rs1006677569

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102789693C>T , CM000673.2:g.102789693C>T GRCh38
NC_000011.9:g.102660424C>T , CM000673.1:g.102660424C>T GRCh37
NC_000011.8:g.102165634C>T NCBI36
NG_011740.1:g.13543G>A
NG_011740.2:g.13543G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000680179.1:n.1307G>A (MMP1)
ENST00000681445.1:n.1303G>A (MMP1)
ENST00000681643.1:n.1329G>A (MMP1)
ENST00000371455.7:n.325-8331C>T (WTAPP1)
ENST00000525739.6:n.390-3452C>T (WTAPP1)
ENST00000544704.1:n.344+5629C>T (WTAPP1)
NR_038390.1:n.390-3452C>T (WTAPP1)