Canonical Allele Identifier: CA1816081160
Gene:

Linked Data

dbSNP Id: rs1563627783

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.122395736G>A , CM000670.2:g.122395736G>A GRCh38
NC_000008.10:g.123407975G>A , CM000670.1:g.123407975G>A GRCh37
NC_000008.9:g.123477156G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_928599.1:n.152+3436C>T
XR_928599.3:n.152+3436C>T