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Canonical Allele Identifier:
CA13505853
Gene: NADSYN1
HGNC
NCBI
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr11:g.71523061G>A
GRCh37
chr11:g.71234107G>A
Linked Data - Sequence & Population
gnomAD v2:
11:71234107 G / A
gnomAD v3:
11:71523061 G / A
gnomAD v4:
chr11-71523061-G-A
Joint Max Group AF
0.32179753 (SAS)
Genomes Max Group AF
0.32179753 (SAS)
Linked Data - NCBI & NCI
dbSNP:
11234027
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.71523061G>A , CM000673.2:g.71523061G>A
GRCh38
NC_000011.9:g.71234107G>A , CM000673.1:g.71234107G>A
GRCh37
NC_000011.8:g.70911755G>A
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
ENST00000527963.1:c.368-935G>A
Search 100 bp 5'
Search 100 bp 3'