Canonical Allele Identifier: CA2293960139
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31756640T= , CM000680.2:g.31756640T= GRCh38
NC_000018.9:g.29336603T= , CM000680.1:g.29336603T= GRCh37
NC_000018.8:g.27590601T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935338.1:n.66-5499T=