Canonical Allele Identifier: CA2724643361

Linked Data

dbSNP Id: rs1857968971

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102789690C>G , CM000673.2:g.102789690C>G GRCh38
NC_000011.9:g.102660421C>G , CM000673.1:g.102660421C>G GRCh37
NC_000011.8:g.102165631C>G NCBI36
NG_011740.1:g.13546G>C
NG_011740.2:g.13546G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000680179.1:n.1310G>C (MMP1)
ENST00000681445.1:n.1306G>C (MMP1)
ENST00000681643.1:n.1332G>C (MMP1)
ENST00000371455.7:n.325-8334C>G (WTAPP1)
ENST00000525739.6:n.390-3455C>G (WTAPP1)
ENST00000544704.1:n.344+5626C>G (WTAPP1)
NR_038390.1:n.390-3455C>G (WTAPP1)