Canonical Allele Identifier: CA1223909937
Gene:

Linked Data

dbSNP Id: rs1655908095

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.224068678C>T , CM000663.2:g.224068678C>T GRCh38
NC_000001.10:g.224256380C>T , CM000663.1:g.224256380C>T GRCh37
NC_000001.9:g.222323003C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_949173.1:n.385+1024C>T
XR_001737824.1:n.242+1024C>T