Canonical Allele Identifier: CA1769514573
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.20734989T= , CM000670.2:g.20734989T= GRCh38
NC_000008.10:g.20592500T= , CM000670.1:g.20592500T= GRCh37
NC_000008.9:g.20636780T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_949569.3:n.72-55457T=