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Canonical Allele Identifier:
CA13787128
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr13:g.42554441T>C
GRCh37
chr13:g.43128577T>C
Linked Data - Sequence & Population
gnomAD v2:
13:43128577 T / C
gnomAD v3:
13:42554441 T / C
gnomAD v4:
chr13-42554441-T-C
Joint Max Group AF
0.43722376 (NFE)
Genomes Max Group AF
0.43722376 (NFE)
Linked Data - NCBI & NCI
dbSNP:
9525638
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000013.11:g.42554441T>C , CM000675.2:g.42554441T>C
GRCh38
NC_000013.10:g.43128577T>C , CM000675.1:g.43128577T>C
GRCh37
NC_000013.9:g.42026577T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'