Canonical Allele Identifier: CA413038146

Gene: RP2

Linked Data

• gnomAD v4: X-46837107-T-A
• MyVariant Identifiers: chrX:g.46696542T>A (hg19) ; chrX:g.46837107T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.46837107T>A , CM000685.2:g.46837107T>A	GRCh38
NC_000023.10:g.46696542T>A , CM000685.1:g.46696542T>A	GRCh37
NC_000023.9:g.46581486T>A	NCBI36
NG_009107.1:g.5196T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218340.4:c.7T>A MANE Select	ENSP00000218340.3:p.Cys3Ser
ENST00000218340.3:c.7T>A	ENSP00000218340.3:p.Cys3Ser
NM_006915.2:c.7T>A	NP_008846.2:p.Cys3Ser
NM_006915.3:c.7T>A MANE Select	NP_008846.2:p.Cys3Ser