Canonical Allele Identifier: CA1816081172
Gene:

Linked Data

dbSNP Id: rs1814946240

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.122395755A>G , CM000670.2:g.122395755A>G GRCh38
NC_000008.10:g.123407994A>G , CM000670.1:g.123407994A>G GRCh37
NC_000008.9:g.123477175A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_928599.1:n.152+3417T>C
XR_928599.3:n.152+3417T>C