Canonical Allele Identifier: CA1146005738
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.213682259G= , CM000663.2:g.213682259G= GRCh38
NC_000001.10:g.213855602G= , CM000663.1:g.213855602G= GRCh37
NC_000001.9:g.211922225G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001738463.1:n.601-49158G=
XR_001738464.1:n.426-49158G=