Canonical Allele Identifier: CA2397661422
Gene: RSPH14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23178964A= , CM000684.2:g.23178964A= GRCh38
NC_000022.10:g.23521151A= , CM000684.1:g.23521151A= GRCh37
NC_000022.9:g.21851151A= NCBI36
NG_009244.1:g.3600A=
NG_009244.2:g.3600A=

Transcript Alleles

HGVS Amino-acid change
XM_017028774.1:c.-53+954T= XP_016884263.1:n.-53+954T=