Canonical Allele Identifier: CA2787761550
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43318661A>G , CM000672.2:g.43318661A>G GRCh38
NC_000010.10:g.43814109A>G , CM000672.1:g.43814109A>G GRCh37
NC_000010.9:g.43134115A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_945902.1:n.108+66A>G
XR_945902.2:n.198+66A>G