Canonical Allele Identifier: CA2615728981

Linked Data

dbSNP Id: rs1858262537

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102798235T>C , CM000673.2:g.102798235T>C GRCh38
NC_000011.9:g.102668966T>C , CM000673.1:g.102668966T>C GRCh37
NC_000011.8:g.102174176T>C NCBI36
NG_011740.1:g.5001A>G
NG_011740.2:g.5001A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371455.7:n.423+113T>C (WTAPP1)
ENST00000525739.6:n.682+113T>C (WTAPP1)
ENST00000544704.1:n.443+113T>C (WTAPP1)
NM_001145938.1:c.-189A>G (MMP1) NP_001139410.1:n.-189A>G
NM_002421.3:c.-143A>G (MMP1) NP_002412.1:n.-143A>G
NR_038390.1:n.682+113T>C (WTAPP1)