Canonical Allele Identifier: CA2197752684
Gene:

Linked Data

dbSNP Id: rs1175541493

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.95782360A>C , CM000677.2:g.95782360A>C GRCh38
NC_000015.9:g.96325589A>C , CM000677.1:g.96325589A>C GRCh37
NC_000015.8:g.94126593A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_932654.1:n.148-42829A>C