Canonical Allele Identifier: CA406404874
Gene: RSPH6A HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.46307656T>C (hg19) chr19:g.45804398T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45804398T>C , CM000681.2:g.45804398T>C GRCh38
NC_000019.9:g.46307656T>C , CM000681.1:g.46307656T>C GRCh37
NC_000019.8:g.50999496T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000221538.8:c.1507A>G MANE Select ENSP00000221538.2:p.Ser503Gly
ENST00000221538.7:c.1507A>G ENSP00000221538.2:p.Ser503Gly
ENST00000597055.1:c.1507A>G ENSP00000472630.1:p.Ser503Gly
ENST00000600188.5:c.715A>G ENSP00000471559.1:p.Ser239Gly
NM_030785.3:c.1507A>G NP_110412.1:p.Ser503Gly
XM_011527351.1:c.1507A>G XP_011525653.1:p.Ser503Gly
XM_011527351.2:c.1507A>G XP_011525653.1:p.Ser503Gly
NM_030785.4:c.1507A>G MANE Select NP_110412.1:p.Ser503Gly
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