Canonical Allele Identifier: CA1052103995
Gene:

Linked Data

dbSNP Id: rs1708399860

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.109743427T>G , CM000665.2:g.109743427T>G GRCh38
NC_000003.11:g.109462274T>G , CM000665.1:g.109462274T>G GRCh37
NC_000003.10:g.110944964T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_924325.1:n.142+63232T>G