Canonical Allele Identifier: CA2615724377

Linked Data

dbSNP Id: rs562503860

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102789877C>G , CM000673.2:g.102789877C>G GRCh38
NC_000011.9:g.102660608C>G , CM000673.1:g.102660608C>G GRCh37
NC_000011.8:g.102165818C>G NCBI36
NG_011740.1:g.13359G>C
NG_011740.2:g.13359G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000680179.1:n.1123G>C (MMP1)
ENST00000681445.1:n.1119G>C (MMP1)
ENST00000681643.1:n.1145G>C (MMP1)
ENST00000371455.7:n.325-8147C>G (WTAPP1)
ENST00000525739.6:n.390-3268C>G (WTAPP1)
ENST00000544704.1:n.344+5813C>G (WTAPP1)
NR_038390.1:n.390-3268C>G (WTAPP1)