Canonical Allele Identifier: CA2065107437
Gene:

Linked Data

dbSNP Id: rs1592921419

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.115398758G>A , CM000674.2:g.115398758G>A GRCh38
NC_000012.11:g.115836563G>A , CM000674.1:g.115836563G>A GRCh37
NC_000012.10:g.114320946G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_945389.1:n.697+8337C>T
XR_945389.2:n.701+8337C>T