Canonical Allele Identifier: CA1223909870
Gene:

Linked Data

dbSNP Id: rs1655905841

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.224068473C>T , CM000663.2:g.224068473C>T GRCh38
NC_000001.10:g.224256175C>T , CM000663.1:g.224256175C>T GRCh37
NC_000001.9:g.222322798C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_949173.1:n.385+819C>T
XR_001737824.1:n.242+819C>T