Canonical Allele Identifier: CA2615728956

Linked Data

dbSNP Id: rs1203768839

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102798223T>A , CM000673.2:g.102798223T>A GRCh38
NC_000011.9:g.102668954T>A , CM000673.1:g.102668954T>A GRCh37
NC_000011.8:g.102174164T>A NCBI36
NG_011740.1:g.5013A>T
NG_011740.2:g.5013A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371455.7:n.423+101T>A (WTAPP1)
ENST00000525739.6:n.682+101T>A (WTAPP1)
ENST00000544704.1:n.443+101T>A (WTAPP1)
NM_001145938.1:c.-177A>T (MMP1) NP_001139410.1:n.-177A>T
NM_002421.3:c.-131A>T (MMP1) NP_002412.1:n.-131A>T
NR_038390.1:n.682+101T>A (WTAPP1)