Canonical Allele Identifier: CA190574840
Gene:
COSMIC:
COSN14918070 (not active)
COSN17445463 (not active)
MyVariant.info:
GRCh38 chr9:g.21035308G>T
GRCh37 chr9:g.21035307G>T
gnomAD v2:
9:21035307 G / T
gnomAD v3:
9:21035308 G / T
gnomAD v4:
chr9-21035308-G-T
Joint Max Group AF 0.6654997 (EAS)
Genomes Max Group AF 0.6654997 (EAS)
dbSNP:
7867456
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21035308G>T , CM000671.2:g.21035308G>T GRCh38
NC_000009.11:g.21035307G>T , CM000671.1:g.21035307G>T GRCh37
NC_000009.10:g.21025307G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_929514.1:n.1210+1812G>T
XR_001746633.1:n.1142+2657G>T
XR_929514.2:n.1276+1812G>T
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