Canonical Allele Identifier: CA941623495

Linked Data

dbSNP Id: rs1857968194

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102789656C>T , CM000673.2:g.102789656C>T GRCh38
NC_000011.9:g.102660387C>T , CM000673.1:g.102660387C>T GRCh37
NC_000011.8:g.102165597C>T NCBI36
NG_011740.1:g.13580G>A
NG_011740.2:g.13580G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000680179.1:n.1344G>A (MMP1)
ENST00000681445.1:n.1340G>A (MMP1)
ENST00000681643.1:n.1366G>A (MMP1)
ENST00000371455.7:n.325-8368C>T (WTAPP1)
ENST00000525739.6:n.390-3489C>T (WTAPP1)
ENST00000544704.1:n.344+5592C>T (WTAPP1)
NR_038390.1:n.390-3489C>T (WTAPP1)