Canonical Allele Identifier: CA185688682
Gene:

Linked Data

dbSNP Id: rs964115751

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.126999625A>G , CM000670.2:g.126999625A>G GRCh38
NC_000008.10:g.128011870A>G , CM000670.1:g.128011870A>G GRCh37
NC_000008.9:g.128081052A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001746076.2:n.1301-6930A>G