Canonical Allele Identifier: CA3731750
Gene: TNXA HGNC NCBI
MyVariant.info:
GRCh38 chr6:g.32010012A>G
GRCh37 chr6:g.31977789A>G
gnomAD v2:
6:31977789 A / G
gnomAD v3:
6:32010012 A / G
gnomAD v4:
chr6-32010012-A-G
Joint Max Group AF 0.11493026 (AFR)
Genomes Max Group AF 0.1144123 (AFR)
Exomes Max Group AF 0.11250501 (AFR)
dbSNP:
10456399
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32010012A>G , CM000668.2:g.32010012A>G GRCh38
NC_000006.11:g.31977789A>G , CM000668.1:g.31977789A>G GRCh37
NC_000006.10:g.32085767A>G NCBI36
NG_011639.1:g.219A>G , LRG_138:g.219A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000507684.1:n.1314T>C
NR_001284.2:n.1865T>C
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