Canonical Allele Identifier: CA1591798701
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.152354516T= , CM000667.2:g.152354516T= GRCh38
NC_000005.9:g.151734077T= , CM000667.1:g.151734077T= GRCh37
NC_000005.8:g.151714270T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_944433.1:n.196+16653T=
XR_944433.2:n.197+16653T=