Canonical Allele Identifier: CA2724643369

Linked Data

dbSNP Id: rs1857969338

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102789710T>C , CM000673.2:g.102789710T>C GRCh38
NC_000011.9:g.102660441T>C , CM000673.1:g.102660441T>C GRCh37
NC_000011.8:g.102165651T>C NCBI36
NG_011740.1:g.13526A>G
NG_011740.2:g.13526A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000680179.1:n.1290A>G (MMP1)
ENST00000681445.1:n.1286A>G (MMP1)
ENST00000681643.1:n.1312A>G (MMP1)
ENST00000371455.7:n.325-8314T>C (WTAPP1)
ENST00000525739.6:n.390-3435T>C (WTAPP1)
ENST00000544704.1:n.344+5646T>C (WTAPP1)
NR_038390.1:n.390-3435T>C (WTAPP1)