Canonical Allele Identifier: CA3731630
Gene: TNXA HGNC NCBI
COSMIC:
COSN19649403 (not active)
MyVariant.info:
GRCh38 chr6:g.32009139C>T
GRCh37 chr6:g.31976916C>T
gnomAD v2:
6:31976916 C / T
gnomAD v3:
6:32009139 C / T
gnomAD v4:
chr6-32009139-C-T
Joint Max Group AF 0.64150751 (AFR)
Genomes Max Group AF 0.63127655 (AFR)
Exomes Max Group AF 0.64972336 (AFR)
dbSNP:
4959083
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32009139C>T , CM000668.2:g.32009139C>T GRCh38
NC_000006.11:g.31976916C>T , CM000668.1:g.31976916C>T GRCh37
NC_000006.10:g.32084894C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000507684.1:n.1833G>A
NR_001284.2:n.2384G>A
Search 100 bp 5'
Search 100 bp 3'