Canonical Allele Identifier: CA2523678569
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.80069250G>T , CM000674.2:g.80069250G>T GRCh38
NC_000012.11:g.80463030G>T , CM000674.1:g.80463030G>T GRCh37
NC_000012.10:g.78987161G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_945140.1:n.456+8068G>T
XR_945141.1:n.1758+8068G>T