Canonical Allele Identifier: CA2025046529
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.29961038C= , CM000674.2:g.29961038C= GRCh38
NC_000012.11:g.30113971C= , CM000674.1:g.30113971C= GRCh37
NC_000012.10:g.30005238C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_931473.1:n.314-17998G=
XR_931474.1:n.314-17998G=
XR_931475.1:n.135-17998G=
XR_001749060.1:n.314-17998G=
XR_001749061.1:n.314-17998G=