Canonical Allele Identifier: CA2197752713
Gene:

Linked Data

dbSNP Id: rs1899531308

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.95782411G>T , CM000677.2:g.95782411G>T GRCh38
NC_000015.9:g.96325640G>T , CM000677.1:g.96325640G>T GRCh37
NC_000015.8:g.94126644G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_932654.1:n.148-42778G>T