Canonical Allele Identifier: CA2293960098
Gene:

Linked Data

dbSNP Id: rs2031431644

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31756542C>A , CM000680.2:g.31756542C>A GRCh38
NC_000018.9:g.29336505C>A , CM000680.1:g.29336505C>A GRCh37
NC_000018.8:g.27590503C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935338.1:n.66-5597C>A