Canonical Allele Identifier: CA1816081351
Gene:

Linked Data

dbSNP Id: rs532631504

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.122396148C>A , CM000670.2:g.122396148C>A GRCh38
NC_000008.10:g.123408387C>A , CM000670.1:g.123408387C>A GRCh37
NC_000008.9:g.123477568C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_928599.1:n.152+3024G>T
XR_928599.3:n.152+3024G>T