Canonical Allele Identifier: CA941623535

Linked Data

dbSNP Id: rs1026886145

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102789725G>A , CM000673.2:g.102789725G>A GRCh38
NC_000011.9:g.102660456G>A , CM000673.1:g.102660456G>A GRCh37
NC_000011.8:g.102165666G>A NCBI36
NG_011740.1:g.13511C>T
NG_011740.2:g.13511C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000680179.1:n.1275C>T (MMP1)
ENST00000681445.1:n.1271C>T (MMP1)
ENST00000681643.1:n.1297C>T (MMP1)
ENST00000371455.7:n.325-8299G>A (WTAPP1)
ENST00000525739.6:n.390-3420G>A (WTAPP1)
ENST00000544704.1:n.344+5661G>A (WTAPP1)
NR_038390.1:n.390-3420G>A (WTAPP1)