Canonical Allele Identifier: CA971148286
Gene:

Linked Data

dbSNP Id: rs1895833341

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.69755841T>G , CM000677.2:g.69755841T>G GRCh38
NC_000015.9:g.70048180T>G , CM000677.1:g.70048180T>G GRCh37
NC_000015.8:g.67835234T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001751592.2:n.86-315T>G