Canonical Allele Identifier: CA2397661423
Gene: RSPH14 HGNC NCBI

Linked Data

dbSNP Id: rs1601976991
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Genomic Alleles

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

Transcript Alleles

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