Canonical Allele Identifier: CA185200389
Gene:

Linked Data

dbSNP Id: rs1010248321

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.122395767C>G , CM000670.2:g.122395767C>G GRCh38
NC_000008.10:g.123408006C>G , CM000670.1:g.123408006C>G GRCh37
NC_000008.9:g.123477187C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_928599.1:n.152+3405G>C
XR_928599.3:n.152+3405G>C