Canonical Allele Identifier: CA670869863

Linked Data

dbSNP Id: rs1163089056

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102789826A>G , CM000673.2:g.102789826A>G GRCh38
NC_000011.9:g.102660557A>G , CM000673.1:g.102660557A>G GRCh37
NC_000011.8:g.102165767A>G NCBI36
NG_011740.1:g.13410T>C
NG_011740.2:g.13410T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000680179.1:n.1174T>C (MMP1)
ENST00000681445.1:n.1170T>C (MMP1)
ENST00000681643.1:n.1196T>C (MMP1)
ENST00000371455.7:n.325-8198A>G (WTAPP1)
ENST00000525739.6:n.390-3319A>G (WTAPP1)
ENST00000544704.1:n.344+5762A>G (WTAPP1)
NR_038390.1:n.390-3319A>G (WTAPP1)