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Canonical Allele Identifier:
CA13532116
Gene: GLYAT
HGNC
NCBI
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.58705326C>A
GRCh37
chr11:g.58472799C>A
Linked Data - Sequence & Population
gnomAD v2:
11:58472799 C / A
gnomAD v3:
11:58705326 C / A
gnomAD v4:
chr11-58705326-C-A
Joint Max Group AF
0.17012508 (AFR)
Genomes Max Group AF
0.17012508 (AFR)
Linked Data - NCBI & NCI
dbSNP:
2507838
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.58705326C>A , CM000673.2:g.58705326C>A
GRCh38
NC_000011.9:g.58472799C>A , CM000673.1:g.58472799C>A
GRCh37
NC_000011.8:g.58229375C>A
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
ENST00000586098.1:c.90+7434G>T
Search 100 bp 5'
Search 100 bp 3'