Canonical Allele Identifier: CA2615724373

Linked Data

dbSNP Id: rs1857973302

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102789876G>A , CM000673.2:g.102789876G>A GRCh38
NC_000011.9:g.102660607G>A , CM000673.1:g.102660607G>A GRCh37
NC_000011.8:g.102165817G>A NCBI36
NG_011740.1:g.13360C>T
NG_011740.2:g.13360C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000680179.1:n.1124C>T (MMP1)
ENST00000681445.1:n.1120C>T (MMP1)
ENST00000681643.1:n.1146C>T (MMP1)
ENST00000371455.7:n.325-8148G>A (WTAPP1)
ENST00000525739.6:n.390-3269G>A (WTAPP1)
ENST00000544704.1:n.344+5812G>A (WTAPP1)
NR_038390.1:n.390-3269G>A (WTAPP1)