Canonical Allele Identifier: CA2293960136
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31756637C= , CM000680.2:g.31756637C= GRCh38
NC_000018.9:g.29336600C= , CM000680.1:g.29336600C= GRCh37
NC_000018.8:g.27590598C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935338.1:n.66-5502C=