Canonical Allele Identifier: CA12756167
Gene: GFRA2 HGNC NCBI
MyVariant.info:
GRCh38 chr8:g.21804933C>A
GRCh37 chr8:g.21662445C>A
gnomAD v2:
8:21662445 C / A
gnomAD v3:
8:21804933 C / A
gnomAD v4:
chr8-21804933-C-A
Joint Max Group AF 0.5363356 (EAS)
Genomes Max Group AF 0.53616115 (EAS)
Exomes Max Group AF 0.2044221 (AFR)
dbSNP:
17581368
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.21804933C>A , CM000670.2:g.21804933C>A GRCh38
NC_000008.10:g.21662445C>A , CM000670.1:g.21662445C>A GRCh37
NC_000008.9:g.21718391C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000517328.5:c.-36+84G>T ENSP00000429445.1:n.-36+84G>T
Search 100 bp 5'
Search 100 bp 3'