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Canonical Allele Identifier:
CA16210586
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr4:g.170056852C>T
GRCh37
chr4:g.170978003C>T
Linked Data - Sequence & Population
gnomAD v2:
4:170978003 C / T
gnomAD v3:
4:170056852 C / T
gnomAD v4:
chr4-170056852-C-T
Joint Max Group AF
0.16689418 (AMR)
Genomes Max Group AF
0.16689418 (AMR)
Linked Data - NCBI & NCI
dbSNP:
4692788
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.170056852C>T , CM000666.2:g.170056852C>T
GRCh38
NC_000004.11:g.170978003C>T , CM000666.1:g.170978003C>T
GRCh37
NC_000004.10:g.171214578C>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_939440.1:n.180C>T
Search 100 bp 5'
Search 100 bp 3'