Canonical Allele Identifier: CA5958571
Gene: CRY2 HGNC NCBI
MyVariant.info:
GRCh38 chr11:g.45856137C>T
GRCh37 chr11:g.45877688C>T
gnomAD v2:
11:45877688 C / T
gnomAD v3:
11:45856137 C / T
gnomAD v4:
chr11-45856137-C-T
Joint Max Group AF 0.00002749 (AFR)
Genomes Max Group AF 0.00001923 (AFR)
Exomes Max Group AF 0.00001108 (AFR)
dbSNP:
2292912
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.45856137C>T , CM000673.2:g.45856137C>T GRCh38
NC_000011.9:g.45877688C>T , CM000673.1:g.45877688C>T GRCh37
NC_000011.8:g.45834264C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000616080.2:c.324+47C>T MANE Select ENSP00000484684.1:n.324+47C>T
ENST00000417225.6:c.141+47C>T ENSP00000397419.2:n.141+47C>T
ENST00000443527.6:c.387+47C>T ENSP00000406751.2:n.387+47C>T
ENST00000473199.5:n.337+47C>T
ENST00000496571.5:n.384C>T
ENST00000532390.5:n.337+47C>T
ENST00000616080.1:c.324+47C>T ENSP00000484684.1:n.324+47C>T
ENST00000616623.4:c.387+47C>T ENSP00000478187.1:n.387+47C>T
NM_001127457.2:c.141+47C>T NP_001120929.1:n.141+47C>T
NM_021117.3:c.387+47C>T NP_066940.2:n.387+47C>T
NM_021117.4:c.324+47C>T NP_066940.3:n.324+47C>T
NM_021117.5:c.324+47C>T MANE Select NP_066940.3:n.324+47C>T
NM_001127457.3:c.141+47C>T NP_001120929.1:n.141+47C>T
Search 100 bp 5'
Search 100 bp 3'