Canonical Allele Identifier: CA1665449787
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.134398893A= , CM000668.2:g.134398893A= GRCh38
NC_000006.11:g.134720031A= , CM000668.1:g.134720031A= GRCh37
NC_000006.10:g.134761724A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_428023.2:n.23+164A=