Canonical Allele Identifier: CA2766279538
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8907063T>C , CM000686.2:g.8907063T>C GRCh38
NC_000024.9:g.8775104T>C , CM000686.1:g.8775104T>C GRCh37
NC_000024.8:g.8835104T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000455422.5:n.110-31T>C