Canonical Allele Identifier: CA2346213813
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.2674200T= , CM000682.2:g.2674200T= GRCh38
NC_000020.10:g.2654846T= , CM000682.1:g.2654846T= GRCh37
NC_000020.9:g.2602846T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_937210.1:n.675-3760A=
XR_937211.1:n.674-3617A=
XR_937210.2:n.668-3760A=
XR_937211.2:n.666-3617A=