Canonical Allele Identifier: CA2549633576
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.7680910T>C , CM000686.2:g.7680910T>C GRCh38
NC_000024.9:g.7548951T>C , CM000686.1:g.7548951T>C GRCh37
NC_000024.8:g.7608951T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000439805.1:n.616+46T>C