Canonical Allele Identifier: CA1580179035
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.126002743T= , CM000667.2:g.126002743T= GRCh38
NC_000005.9:g.125338436T= , CM000667.1:g.125338436T= GRCh37
NC_000005.8:g.125366335T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_948737.1:n.565+3597A=
XR_948738.1:n.497+5797A=