Canonical Allele Identifier: CA2025046494
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.29960952G= , CM000674.2:g.29960952G= GRCh38
NC_000012.11:g.30113885G= , CM000674.1:g.30113885G= GRCh37
NC_000012.10:g.30005152G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_931473.1:n.314-17912C=
XR_931474.1:n.314-17912C=
XR_931475.1:n.135-17912C=
XR_001749060.1:n.314-17912C=
XR_001749061.1:n.314-17912C=