Canonical Allele Identifier: CA2559966388
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.28544554G>A , CM000681.2:g.28544554G>A GRCh38
NC_000019.9:g.29035461G>A , CM000681.1:g.29035461G>A GRCh37
NC_000019.8:g.33727301G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110759.1:n.657-77774C>T
XR_243979.1:n.110-51531C>T