Canonical Allele Identifier: CA2031042722
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40373572C= , CM000674.2:g.40373572C= GRCh38
NC_000012.11:g.40767374C= , CM000674.1:g.40767374C= GRCh37
NC_000012.10:g.39053641C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_944868.1:n.485-18745G=
XR_944869.1:n.485-1520G=
XR_001749087.1:n.380-1520G=
XR_001749088.1:n.347-1520G=
XR_944868.2:n.485-18745G=
XR_944869.2:n.485-1520G=