Canonical Allele Identifier: CA2031042761
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40373613C= , CM000674.2:g.40373613C= GRCh38
NC_000012.11:g.40767415C= , CM000674.1:g.40767415C= GRCh37
NC_000012.10:g.39053682C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_944868.1:n.485-18786G=
XR_944869.1:n.485-1561G=
XR_001749087.1:n.380-1561G=
XR_001749088.1:n.347-1561G=
XR_944868.2:n.485-18786G=
XR_944869.2:n.485-1561G=