Canonical Allele Identifier: CA9522666
Gene: RSPH6A HGNC NCBI

Linked Data

dbSNP Id: rs774360093

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45804445C>T , CM000681.2:g.45804445C>T GRCh38
NC_000019.9:g.46307703C>T , CM000681.1:g.46307703C>T GRCh37
NC_000019.8:g.50999543C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000221538.8:c.1460G>A MANE Select ENSP00000221538.2:p.Arg487His
ENST00000221538.7:c.1460G>A ENSP00000221538.2:p.Arg487His
ENST00000597055.1:c.1460G>A ENSP00000472630.1:p.Arg487His
ENST00000600188.5:c.668G>A ENSP00000471559.1:p.Arg223His
NM_030785.3:c.1460G>A NP_110412.1:p.Arg487His
XM_011527351.1:c.1460G>A XP_011525653.1:p.Arg487His
XM_011527351.2:c.1460G>A XP_011525653.1:p.Arg487His
NM_030785.4:c.1460G>A MANE Select NP_110412.1:p.Arg487His