Canonical Allele Identifier: CA2592914353
Gene:

Linked Data

dbSNP Id: rs2143936434

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.41477544C>A , CM000680.2:g.41477544C>A GRCh38
NC_000018.9:g.39057508C>A , CM000680.1:g.39057508C>A GRCh37
NC_000018.8:g.37311506C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935409.1:n.86-26590C>A