Canonical Allele Identifier: CA1223909901
Gene:

Linked Data

dbSNP Id: rs1655906932

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.224068577T>C , CM000663.2:g.224068577T>C GRCh38
NC_000001.10:g.224256279T>C , CM000663.1:g.224256279T>C GRCh37
NC_000001.9:g.222322902T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_949173.1:n.385+923T>C
XR_001737824.1:n.242+923T>C