Canonical Allele Identifier: CA2721136853
Gene:

Linked Data

dbSNP Id: rs1170457396

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30201631G>T , CM000672.2:g.30201631G>T GRCh38
NC_000010.10:g.30490560G>T , CM000672.1:g.30490560G>T GRCh37
NC_000010.9:g.30530566G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930791.1:n.1193-1856G>T
XR_930791.2:n.1449-1856G>T