Canonical Allele Identifier: CA2224227964
Gene:

Linked Data

dbSNP Id: rs1960021153

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56610690T>C , CM000678.2:g.56610690T>C GRCh38
NC_000016.9:g.56644602T>C , CM000678.1:g.56644602T>C GRCh37
NC_000016.8:g.55202103T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_933616.1:n.605+626A>G