Canonical Allele Identifier: CA298296858
Gene:

Linked Data

dbSNP Id: rs193200973

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31756656T>A , CM000680.2:g.31756656T>A GRCh38
NC_000018.9:g.29336619T>A , CM000680.1:g.29336619T>A GRCh37
NC_000018.8:g.27590617T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935338.1:n.66-5483T>A