Canonical Allele Identifier: CA406404910

Gene: RSPH6A

Linked Data

• dbSNP Id: rs1970512216
• gnomAD v3: 19-45804412-C-T
• gnomAD v4: 19-45804412-C-T
• MyVariant Identifiers: chr19:g.46307670C>T (hg19) ; chr19:g.45804412C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45804412C>T , CM000681.2:g.45804412C>T	GRCh38
NC_000019.9:g.46307670C>T , CM000681.1:g.46307670C>T	GRCh37
NC_000019.8:g.50999510C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221538.8:c.1493G>A MANE Select	ENSP00000221538.2:p.Gly498Asp
ENST00000221538.7:c.1493G>A	ENSP00000221538.2:p.Gly498Asp
ENST00000597055.1:c.1493G>A	ENSP00000472630.1:p.Gly498Asp
ENST00000600188.5:c.701G>A	ENSP00000471559.1:p.Gly234Asp
NM_030785.3:c.1493G>A	NP_110412.1:p.Gly498Asp
XM_011527351.1:c.1493G>A	XP_011525653.1:p.Gly498Asp
XM_011527351.2:c.1493G>A	XP_011525653.1:p.Gly498Asp
NM_030785.4:c.1493G>A MANE Select	NP_110412.1:p.Gly498Asp