Canonical Allele Identifier: CA2709162089
Gene:

Linked Data

dbSNP Id: rs2112035120

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.66487833C>T , CM000667.2:g.66487833C>T GRCh38
NC_000005.9:g.65783661C>T , CM000667.1:g.65783661C>T GRCh37
NC_000005.8:g.65819417C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_948381.1:n.649-49003C>T