Canonical Allele Identifier: CA2025046513
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.29961006G= , CM000674.2:g.29961006G= GRCh38
NC_000012.11:g.30113939G= , CM000674.1:g.30113939G= GRCh37
NC_000012.10:g.30005206G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_931473.1:n.314-17966C=
XR_931474.1:n.314-17966C=
XR_931475.1:n.135-17966C=
XR_001749060.1:n.314-17966C=
XR_001749061.1:n.314-17966C=