Canonical Allele Identifier: CA406404870
Gene: RSPH6A HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.46307654A>T (hg19) chr19:g.45804396A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45804396A>T , CM000681.2:g.45804396A>T GRCh38
NC_000019.9:g.46307654A>T , CM000681.1:g.46307654A>T GRCh37
NC_000019.8:g.50999494A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000221538.8:c.1509T>A MANE Select ENSP00000221538.2:p.Ser503Arg
ENST00000221538.7:c.1509T>A ENSP00000221538.2:p.Ser503Arg
ENST00000597055.1:c.1509T>A ENSP00000472630.1:p.Ser503Arg
ENST00000600188.5:c.717T>A ENSP00000471559.1:p.Ser239Arg
NM_030785.3:c.1509T>A NP_110412.1:p.Ser503Arg
XM_011527351.1:c.1509T>A XP_011525653.1:p.Ser503Arg
XM_011527351.2:c.1509T>A XP_011525653.1:p.Ser503Arg
NM_030785.4:c.1509T>A MANE Select NP_110412.1:p.Ser503Arg
Search 100 bp 5'
Search 100 bp 3'