Canonical Allele Identifier: CA2025046525
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.29961028T= , CM000674.2:g.29961028T= GRCh38
NC_000012.11:g.30113961T= , CM000674.1:g.30113961T= GRCh37
NC_000012.10:g.30005228T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_931473.1:n.314-17988A=
XR_931474.1:n.314-17988A=
XR_931475.1:n.135-17988A=
XR_001749060.1:n.314-17988A=
XR_001749061.1:n.314-17988A=