Canonical Allele Identifier: CA413038340

Gene: RP2

Linked Data

• gnomAD v4: X-46837186-G-A
• MyVariant Identifiers: chrX:g.46696621G>A (hg19) ; chrX:g.46837186G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.46837186G>A , CM000685.2:g.46837186G>A	GRCh38
NC_000023.10:g.46696621G>A , CM000685.1:g.46696621G>A	GRCh37
NC_000023.9:g.46581565G>A	NCBI36
NG_009107.1:g.5275G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218340.4:c.86G>A MANE Select	ENSP00000218340.3:p.Trp29Ter
ENST00000218340.3:c.86G>A	ENSP00000218340.3:p.Trp29Ter
NM_006915.2:c.86G>A	NP_008846.2:p.Trp29Ter
NM_006915.3:c.86G>A MANE Select	NP_008846.2:p.Trp29Ter