Canonical Allele Identifier: CA2049072576
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.80069424A= , CM000674.2:g.80069424A= GRCh38
NC_000012.11:g.80463204A= , CM000674.1:g.80463204A= GRCh37
NC_000012.10:g.78987335A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945140.1:n.456+8242A=
XR_945141.1:n.1758+8242A=