Canonical Allele Identifier: CA666858115
Gene:

Linked Data

dbSNP Id: rs1296905353

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.57812991G>T , CM000672.2:g.57812991G>T GRCh38
NC_000010.10:g.59572751G>T , CM000672.1:g.59572751G>T GRCh37
NC_000010.9:g.59242757G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_945979.1:n.68+34301C>A
XR_001747454.1:n.85+34301C>A