Canonical Allele Identifier: CA13017001
Gene:
MyVariant.info:
GRCh38 chr9:g.104928714G>A
GRCh37 chr9:g.107690995G>A
gnomAD v2:
9:107690995 G / A
gnomAD v3:
9:104928714 G / A
gnomAD v4:
chr9-104928714-G-A
Joint Max Group AF 0.52518059 (AMR)
Genomes Max Group AF 0.52518059 (AMR)
Exomes Max Group AF 0.30228302 (NFE)
dbSNP:
2422493
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.104928714G>A , CM000671.2:g.104928714G>A GRCh38
NC_000009.11:g.107690995G>A , CM000671.1:g.107690995G>A GRCh37
NC_000009.10:g.106730816G>A NCBI36
NG_007981.1:g.4442C>T

Transcript Alleles

HGVS Amino-acid Change
XR_930204.1:n.735-794G>A
XR_930204.2:n.116-794G>A
Search 100 bp 5'
Search 100 bp 3'