Canonical Allele Identifier: CA2339606549
Gene: CRX HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47834564T= , CM000681.2:g.47834564T= GRCh38
NC_000019.9:g.48337821T= , CM000681.1:g.48337821T= GRCh37
NC_000019.8:g.53029633T= NCBI36
NG_008605.1:g.17723T=

Transcript Alleles

HGVS Amino-acid change
ENST00000221996.12:c.100+21T= MANE Select ENSP00000221996.5:n.100+21T=
ENST00000221996.11:c.100+21T= ENSP00000221996.5:n.100+21T=
ENST00000539067.5:c.100+21T= ENSP00000445565.1:n.100+21T=
ENST00000556527.1:n.78-1679T=
ENST00000566686.5:c.100+21T= ENSP00000457808.2:n.100+21T=
ENST00000613299.1:c.100+21T= ENSP00000478106.1:n.100+21T=
NM_000554.4:c.100+21T= NP_000545.1:n.100+21T=
NM_000554.5:c.100+21T= NP_000545.1:n.100+21T=
NM_000554.6:c.100+21T= MANE Select NP_000545.1:n.100+21T=
Search 100 bp 5'
Search 100 bp 3'