Canonical Allele Identifier: CA2839699667
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.69755847T>G , CM000677.2:g.69755847T>G GRCh38
NC_000015.9:g.70048186T>G , CM000677.1:g.70048186T>G GRCh37
NC_000015.8:g.67835240T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001751592.2:n.86-309T>G