Canonical Allele Identifier: CA10652641

Gene: CRX

Linked Data

• ClinVar Variation Id: 329755
• ClinVar RCV Id: RCV000279799 ; RCV000318530 ; RCV000372070
• dbSNP Id: rs181823708
• gnomAD v2: 19-48345361-G-A
• gnomAD v3: 19-47842104-G-A
• gnomAD v4: 19-47842104-G-A
• MyVariant Identifiers: chr19:g.48345361G>A (hg19) ; chr19:g.47842104G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.47842104G>A , CM000681.2:g.47842104G>A	GRCh38
NC_000019.9:g.48345361G>A , CM000681.1:g.48345361G>A	GRCh37
NC_000019.8:g.53037173G>A	NCBI36
NG_008605.1:g.25263G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221996.12:c.*2137G>A MANE Select	ENSP00000221996.5:n.*2137G>A
ENST00000221996.11:c.*2137G>A	ENSP00000221996.5:n.*2137G>A
ENST00000539067.5:c.*467-450G>A	ENSP00000445565.1:n.*467-450G>A
ENST00000602001.1:n.46-408G>A
ENST00000613299.1:c.*2759G>A	ENSP00000478106.1:n.*2759G>A
NM_000554.4:c.*2137G>A	NP_000545.1:n.*2137G>A
NM_000554.5:c.*2137G>A	NP_000545.1:n.*2137G>A
NM_000554.6:c.*2137G>A MANE Select	NP_000545.1:n.*2137G>A