Canonical Allele Identifier: CA2049072532
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.80069328T= , CM000674.2:g.80069328T= GRCh38
NC_000012.11:g.80463108T= , CM000674.1:g.80463108T= GRCh37
NC_000012.10:g.78987239T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_945140.1:n.456+8146T=
XR_945141.1:n.1758+8146T=