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Canonical Allele Identifier:
CA11357572
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr3:g.35101019G>T
GRCh37
chr3:g.35142511G>T
Linked Data - Sequence & Population
gnomAD v2:
3:35142511 G / T
gnomAD v3:
3:35101019 G / T
gnomAD v4:
chr3-35101019-G-T
Joint Max Group AF
0.33944982 (SAS)
Genomes Max Group AF
0.33944982 (SAS)
Linked Data - NCBI & NCI
dbSNP:
11129640
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.35101019G>T , CM000665.2:g.35101019G>T
GRCh38
NC_000003.11:g.35142511G>T , CM000665.1:g.35142511G>T
GRCh37
NC_000003.10:g.35117515G>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_110817.1:n.206+205452C>A
Search 100 bp 5'
Search 100 bp 3'