Canonical Allele Identifier: CA2519616659
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.32890319T>G , CM000683.2:g.32890319T>G GRCh38
NC_000021.8:g.34262627T>G , CM000683.1:g.34262627T>G GRCh37
NC_000021.7:g.33184497T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_937669.1:n.460-3259T>G
XR_937669.2:n.1038-3259T>G