Canonical Allele Identifier: CA2298481208
Gene:

Linked Data

dbSNP Id: rs1910117766

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.41477618T>C , CM000680.2:g.41477618T>C GRCh38
NC_000018.9:g.39057582T>C , CM000680.1:g.39057582T>C GRCh37
NC_000018.8:g.37311580T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935409.1:n.86-26516T>C