Canonical Allele Identifier: CA2284239383
Gene:

Linked Data

dbSNP Id: rs1598367313

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10321316T>C , CM000680.2:g.10321316T>C GRCh38
NC_000018.9:g.10321313T>C , CM000680.1:g.10321313T>C GRCh37
NC_000018.8:g.10311313T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935138.1:n.665+832A>G
XR_001753344.1:n.650+832A>G
XR_001753345.1:n.805A>G
XR_001753346.1:n.549+832A>G