Canonical Allele Identifier: CA2580598338
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43318601G>C , CM000672.2:g.43318601G>C GRCh38
NC_000010.10:g.43814049G>C , CM000672.1:g.43814049G>C GRCh37
NC_000010.9:g.43134055G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_945902.1:n.108+6G>C
XR_945902.2:n.198+6G>C