Canonical Allele Identifier: CA227359892

Linked Data

dbSNP Id: rs1026585990

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102789888G>C , CM000673.2:g.102789888G>C GRCh38
NC_000011.9:g.102660619G>C , CM000673.1:g.102660619G>C GRCh37
NC_000011.8:g.102165829G>C NCBI36
NG_011740.1:g.13348C>G
NG_011740.2:g.13348C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000680179.1:n.1112C>G (MMP1)
ENST00000681445.1:n.1108C>G (MMP1)
ENST00000681643.1:n.1134C>G (MMP1)
ENST00000371455.7:n.325-8136G>C (WTAPP1)
ENST00000525739.6:n.390-3257G>C (WTAPP1)
ENST00000544704.1:n.344+5824G>C (WTAPP1)
NR_038390.1:n.390-3257G>C (WTAPP1)