Canonical Allele Identifier: CA545410444
Gene:

Linked Data

dbSNP Id: rs1314958302

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.109743567T>G , CM000665.2:g.109743567T>G GRCh38
NC_000003.11:g.109462414T>G , CM000665.1:g.109462414T>G GRCh37
NC_000003.10:g.110945104T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_924325.1:n.142+63372T>G