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Canonical Allele Identifier:
CA11360122
Gene: CCRL2
HGNC
NCBI
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr3:g.46410189A>G
GRCh37
chr3:g.46451680A>G
Linked Data - Sequence & Population
gnomAD v2:
3:46451680 A / G
gnomAD v3:
3:46410189 A / G
gnomAD v4:
chr3-46410189-A-G
Joint Max Group AF
0.89669053 (AFR)
Genomes Max Group AF
0.89669053 (AFR)
Linked Data - NCBI & NCI
dbSNP:
1015164
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.46410189A>G , CM000665.2:g.46410189A>G
GRCh38
NC_000003.11:g.46451680A>G , CM000665.1:g.46451680A>G
GRCh37
NC_000003.10:g.46426684A>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
ENST00000441909.1:n.167+509A>G
Search 100 bp 5'
Search 100 bp 3'