Canonical Allele Identifier: CA601245909

Linked Data

dbSNP Id: rs1328966948

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102789657G>A , CM000673.2:g.102789657G>A GRCh38
NC_000011.9:g.102660388G>A , CM000673.1:g.102660388G>A GRCh37
NC_000011.8:g.102165598G>A NCBI36
NG_011740.1:g.13579C>T
NG_011740.2:g.13579C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000680179.1:n.1343C>T (MMP1)
ENST00000681445.1:n.1339C>T (MMP1)
ENST00000681643.1:n.1365C>T (MMP1)
ENST00000371455.7:n.325-8367G>A (WTAPP1)
ENST00000525739.6:n.390-3488G>A (WTAPP1)
ENST00000544704.1:n.344+5593G>A (WTAPP1)
NR_038390.1:n.390-3488G>A (WTAPP1)