Canonical Allele Identifier: CA2116164768
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.104826302T= , CM000675.2:g.104826302T= GRCh38
NC_000013.10:g.105478653T= , CM000675.1:g.105478653T= GRCh37
NC_000013.9:g.104276654T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001749993.1:n.242-2515A=
XR_001749994.1:n.243+10901A=
XR_001749995.1:n.253+10901A=
XR_001749996.1:n.1897-2753T=