Canonical Allele Identifier: CA2116164780
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.104826335C= , CM000675.2:g.104826335C= GRCh38
NC_000013.10:g.105478686C= , CM000675.1:g.105478686C= GRCh37
NC_000013.9:g.104276687C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001749993.1:n.242-2548G=
XR_001749994.1:n.243+10868G=
XR_001749995.1:n.253+10868G=
XR_001749996.1:n.1897-2720C=