Canonical Allele Identifier: CA1563552129
Gene:

Linked Data

dbSNP Id: rs1744565685

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.92222890G>T , CM000667.2:g.92222890G>T GRCh38
NC_000005.9:g.91518707G>T , CM000667.1:g.91518707G>T GRCh37
NC_000005.8:g.91554463G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_948565.1:n.394+18206G>T