Canonical Allele Identifier: CA2293960307
Gene:

Linked Data

dbSNP Id: rs1257868655

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31757031A>G , CM000680.2:g.31757031A>G GRCh38
NC_000018.9:g.29336994A>G , CM000680.1:g.29336994A>G GRCh37
NC_000018.8:g.27590992A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935338.1:n.66-5108A>G