Canonical Allele Identifier: CA941623516

Linked Data

dbSNP Id: rs1857969484

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102789715C>A , CM000673.2:g.102789715C>A GRCh38
NC_000011.9:g.102660446C>A , CM000673.1:g.102660446C>A GRCh37
NC_000011.8:g.102165656C>A NCBI36
NG_011740.1:g.13521G>T
NG_011740.2:g.13521G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000680179.1:n.1285G>T (MMP1)
ENST00000681445.1:n.1281G>T (MMP1)
ENST00000681643.1:n.1307G>T (MMP1)
ENST00000371455.7:n.325-8309C>A (WTAPP1)
ENST00000525739.6:n.390-3430C>A (WTAPP1)
ENST00000544704.1:n.344+5651C>A (WTAPP1)
NR_038390.1:n.390-3430C>A (WTAPP1)