Canonical Allele Identifier: CA778454206
Gene:

Linked Data

dbSNP Id: rs1419242773

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31756651C>A , CM000680.2:g.31756651C>A GRCh38
NC_000018.9:g.29336614C>A , CM000680.1:g.29336614C>A GRCh37
NC_000018.8:g.27590612C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935338.1:n.66-5488C>A