ClinGen Allele Registry
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Canonical Allele Identifier:
CA15314686
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.11628425T>C
GRCh37
chr4:g.11630049T>C
Linked Data - Sequence & Population
gnomAD v2:
4:11630049 T / C
gnomAD v3:
4:11628425 T / C
gnomAD v4:
chr4-11628425-T-C
Joint Max Group AF
0.89476293 (AFR)
Genomes Max Group AF
0.89476293 (AFR)
Linked Data - NCBI & NCI
dbSNP:
6448799
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.11628425T>C , CM000666.2:g.11628425T>C
GRCh38
NC_000004.11:g.11630049T>C , CM000666.1:g.11630049T>C
GRCh37
NC_000004.10:g.11239147T>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_001741361.1:n.1026+76471T>C
Search 100 bp 5'
Search 100 bp 3'