Canonical Allele Identifier: CA2116164779
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.104826334G= , CM000675.2:g.104826334G= GRCh38
NC_000013.10:g.105478685G= , CM000675.1:g.105478685G= GRCh37
NC_000013.9:g.104276686G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001749993.1:n.242-2547C=
XR_001749994.1:n.243+10869C=
XR_001749995.1:n.253+10869C=
XR_001749996.1:n.1897-2721G=