Canonical Allele Identifier: CA8211636
Gene: CRISPLD2 HGNC NCBI
MyVariant.info:
GRCh38 chr16:g.84854704C>T
GRCh37 chr16:g.84888310C>T
gnomAD v2:
16:84888310 C / T
gnomAD v3:
16:84854704 C / T
gnomAD v4:
chr16-84854704-C-T
Joint Max Group AF 0.47504562 (EAS)
Genomes Max Group AF 0.48178639 (EAS)
Exomes Max Group AF 0.47244927 (EAS)
dbSNP:
4782675
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.84854704C>T , CM000678.2:g.84854704C>T GRCh38
NC_000016.9:g.84888310C>T , CM000678.1:g.84888310C>T GRCh37
NC_000016.8:g.83445811C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000262424.10:c.609-25C>T MANE Select ENSP00000262424.5:n.609-25C>T
ENST00000262424.9:c.609-25C>T ENSP00000262424.5:n.609-25C>T
ENST00000563066.5:c.138-25C>T ENSP00000456952.1:n.138-25C>T
ENST00000564567.5:c.609-25C>T ENSP00000457655.1:n.609-25C>T
ENST00000566431.5:n.825-25C>T
ENST00000566789.1:c.138-25C>T ENSP00000457259.1:n.138-25C>T
ENST00000567845.5:c.609-25C>T ENSP00000457183.1:n.609-25C>T
ENST00000569262.5:n.800-25C>T
NM_031476.3:c.609-25C>T NP_113664.1:n.609-25C>T
XM_005256190.1:c.609-25C>T XP_005256247.1:n.609-25C>T
XM_024450463.1:c.609-25C>T XP_024306231.1:n.609-25C>T
NM_031476.4:c.609-25C>T MANE Select NP_113664.1:n.609-25C>T
Search 100 bp 5'
Search 100 bp 3'