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Canonical Allele Identifier:
CA12277599
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.113745925T>C
GRCh37
chr6:g.114067127T>C
Linked Data - Sequence & Population
gnomAD v2:
6:114067127 T / C
gnomAD v3:
6:113745925 T / C
gnomAD v4:
chr6-113745925-T-C
Joint Max Group AF
0.50435186 (AFR)
Genomes Max Group AF
0.50435186 (AFR)
Linked Data - NCBI & NCI
dbSNP:
2030926
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.113745925T>C , CM000668.2:g.113745925T>C
GRCh38
NC_000006.11:g.114067127T>C , CM000668.1:g.114067127T>C
GRCh37
NC_000006.10:g.114173820T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'