Canonical Allele Identifier: CA2031042649
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40373522C= , CM000674.2:g.40373522C= GRCh38
NC_000012.11:g.40767324C= , CM000674.1:g.40767324C= GRCh37
NC_000012.10:g.39053591C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_944868.1:n.485-18695G=
XR_944869.1:n.485-1470G=
XR_001749087.1:n.380-1470G=
XR_001749088.1:n.347-1470G=
XR_944868.2:n.485-18695G=
XR_944869.2:n.485-1470G=