Canonical Allele Identifier: CA2284239331
Gene:

Linked Data

dbSNP Id: rs1036840433

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10321226G>C , CM000680.2:g.10321226G>C GRCh38
NC_000018.9:g.10321223G>C , CM000680.1:g.10321223G>C GRCh37
NC_000018.8:g.10311223G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935138.1:n.665+922C>G
XR_001753344.1:n.650+922C>G
XR_001753345.1:n.895C>G
XR_001753346.1:n.549+922C>G