Canonical Allele Identifier: CA227359697

Linked Data

dbSNP Id: rs17099570

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102789653G>C , CM000673.2:g.102789653G>C GRCh38
NC_000011.9:g.102660384G>C , CM000673.1:g.102660384G>C GRCh37
NC_000011.8:g.102165594G>C NCBI36
NG_011740.1:g.13583C>G
NG_011740.2:g.13583C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000680179.1:n.1347C>G (MMP1)
ENST00000681445.1:n.1343C>G (MMP1)
ENST00000681643.1:n.1369C>G (MMP1)
ENST00000371455.7:n.325-8371G>C (WTAPP1)
ENST00000525739.6:n.390-3492G>C (WTAPP1)
ENST00000544704.1:n.344+5589G>C (WTAPP1)
NR_038390.1:n.390-3492G>C (WTAPP1)