Canonical Allele Identifier: CA1905920007
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43318623A= , CM000672.2:g.43318623A= GRCh38
NC_000010.10:g.43814071A= , CM000672.1:g.43814071A= GRCh37
NC_000010.9:g.43134077A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945902.1:n.108+28A=
XR_945902.2:n.198+28A=