Canonical Allele Identifier: CA227359875

Linked Data

dbSNP Id: rs932546635

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102789841C>G , CM000673.2:g.102789841C>G GRCh38
NC_000011.9:g.102660572C>G , CM000673.1:g.102660572C>G GRCh37
NC_000011.8:g.102165782C>G NCBI36
NG_011740.1:g.13395G>C
NG_011740.2:g.13395G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000680179.1:n.1159G>C (MMP1)
ENST00000681445.1:n.1155G>C (MMP1)
ENST00000681643.1:n.1181G>C (MMP1)
ENST00000371455.7:n.325-8183C>G (WTAPP1)
ENST00000525739.6:n.390-3304C>G (WTAPP1)
ENST00000544704.1:n.344+5777C>G (WTAPP1)
NR_038390.1:n.390-3304C>G (WTAPP1)