ClinGen Allele Registry
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Canonical Allele Identifier:
CA907548962
Gene: CCRL2
HGNC
NCBI
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr3:g.46410189A>T
GRCh37
chr3:g.46451680A>T
Linked Data - Sequence & Population
gnomAD v3:
3:46410189 A / T
gnomAD v4:
chr3-46410189-A-T
Linked Data - NCBI & NCI
dbSNP:
1015164
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.46410189A>T , CM000665.2:g.46410189A>T
GRCh38
NC_000003.11:g.46451680A>T , CM000665.1:g.46451680A>T
GRCh37
NC_000003.10:g.46426684A>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
ENST00000441909.1:n.167+509A>T
Search 100 bp 5'
Search 100 bp 3'