Canonical Allele Identifier: CA11890460
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52545963G>A , CM000666.2:g.52545963G>A GRCh38
NC_000004.11:g.53412129G>A , CM000666.1:g.53412129G>A GRCh37
NC_000004.10:g.53106886G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_002959792.1:n.202+5510C>T
XR_002959793.1:n.202+5510C>T