Canonical Allele Identifier: CA601245908

Linked Data

dbSNP Id: rs1419422307

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102789648A>G , CM000673.2:g.102789648A>G GRCh38
NC_000011.9:g.102660379A>G , CM000673.1:g.102660379A>G GRCh37
NC_000011.8:g.102165589A>G NCBI36
NG_011740.1:g.13588T>C
NG_011740.2:g.13588T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000680179.1:n.1352T>C (MMP1)
ENST00000681445.1:n.1348T>C (MMP1)
ENST00000681643.1:n.1374T>C (MMP1)
ENST00000371455.7:n.325-8376A>G (WTAPP1)
ENST00000525739.6:n.390-3497A>G (WTAPP1)
ENST00000544704.1:n.344+5584A>G (WTAPP1)
NR_038390.1:n.390-3497A>G (WTAPP1)