Canonical Allele Identifier: CA298296859
Gene:

Linked Data

dbSNP Id: rs1000168699

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31756665T>C , CM000680.2:g.31756665T>C GRCh38
NC_000018.9:g.29336628T>C , CM000680.1:g.29336628T>C GRCh37
NC_000018.8:g.27590626T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935338.1:n.66-5474T>C