Canonical Allele Identifier: CA941623559

Linked Data

dbSNP Id: rs1857972186

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102789831G>T , CM000673.2:g.102789831G>T GRCh38
NC_000011.9:g.102660562G>T , CM000673.1:g.102660562G>T GRCh37
NC_000011.8:g.102165772G>T NCBI36
NG_011740.1:g.13405C>A
NG_011740.2:g.13405C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000680179.1:n.1169C>A (MMP1)
ENST00000681445.1:n.1165C>A (MMP1)
ENST00000681643.1:n.1191C>A (MMP1)
ENST00000371455.7:n.325-8193G>T (WTAPP1)
ENST00000525739.6:n.390-3314G>T (WTAPP1)
ENST00000544704.1:n.344+5767G>T (WTAPP1)
NR_038390.1:n.390-3314G>T (WTAPP1)