Canonical Allele Identifier: CA2049072475
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.80069215G= , CM000674.2:g.80069215G= GRCh38
NC_000012.11:g.80462995G= , CM000674.1:g.80462995G= GRCh37
NC_000012.10:g.78987126G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_945140.1:n.456+8033G=
XR_945141.1:n.1758+8033G=