Canonical Allele Identifier: CA3731633
Gene: TNXA HGNC NCBI
COSMIC:
COSN14895063 (not active)
COSN19614252 (not active)
COSN19625584 (not active)
COSN19633157 (not active)
MyVariant.info:
GRCh38 chr6:g.32009149C>T
GRCh37 chr6:g.31976926C>T
gnomAD v2:
6:31976926 C / T
gnomAD v3:
6:32009149 C / T
gnomAD v4:
chr6-32009149-C-T
Joint Max Group AF 0.63957925 (AFR)
Genomes Max Group AF 0.62606673 (AFR)
Exomes Max Group AF 0.65195078 (AFR)
dbSNP:
4959084
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32009149C>T , CM000668.2:g.32009149C>T GRCh38
NC_000006.11:g.31976926C>T , CM000668.1:g.31976926C>T GRCh37
NC_000006.10:g.32084904C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000507684.1:n.1823G>A
NR_001284.2:n.2374G>A
Search 100 bp 5'
Search 100 bp 3'