Canonical Allele Identifier: CA2185570199
Gene:

Linked Data

dbSNP Id: rs1895832260

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.69755769C>A , CM000677.2:g.69755769C>A GRCh38
NC_000015.9:g.70048108C>A , CM000677.1:g.70048108C>A GRCh37
NC_000015.8:g.67835162C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001751592.2:n.86-387C>A