Canonical Allele Identifier: CA10652167
Gene: CRX HGNC NCBI

Linked Data

ClinVar Variation Id: 329753
dbSNP Id: rs12982537

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47842073C>T , CM000681.2:g.47842073C>T GRCh38
NC_000019.9:g.48345330C>T , CM000681.1:g.48345330C>T GRCh37
NC_000019.8:g.53037142C>T NCBI36
NG_008605.1:g.25232C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000221996.12:c.*2106C>T MANE Select ENSP00000221996.5:n.*2106C>T
ENST00000221996.11:c.*2106C>T ENSP00000221996.5:n.*2106C>T
ENST00000539067.5:c.*467-481C>T ENSP00000445565.1:n.*467-481C>T
ENST00000602001.1:n.46-439C>T
ENST00000613299.1:c.*2728C>T ENSP00000478106.1:n.*2728C>T
NM_000554.4:c.*2106C>T NP_000545.1:n.*2106C>T
NM_000554.5:c.*2106C>T NP_000545.1:n.*2106C>T
NM_000554.6:c.*2106C>T MANE Select NP_000545.1:n.*2106C>T