Canonical Allele Identifier: CA2469949916
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.7680917G= , CM000686.2:g.7680917G= GRCh38
NC_000024.9:g.7548958G= , CM000686.1:g.7548958G= GRCh37
NC_000024.8:g.7608958G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000439805.1:n.616+53G=