Canonical Allele Identifier: CA1118643318
Gene:

Linked Data

dbSNP Id: rs1814947316

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.122395818C>T , CM000670.2:g.122395818C>T GRCh38
NC_000008.10:g.123408057C>T , CM000670.1:g.123408057C>T GRCh37
NC_000008.9:g.123477238C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_928599.1:n.152+3354G>A
XR_928599.3:n.152+3354G>A