Canonical Allele Identifier: CA2024154229
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.28045195A= , CM000674.2:g.28045195A= GRCh38
NC_000012.11:g.28198128A= , CM000674.1:g.28198128A= GRCh37
NC_000012.10:g.28089395A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_931460.1:n.154-6237T=