Canonical Allele Identifier: CA3731750
Gene: TNXA HGNC NCBI

Linked Data

dbSNP Id: rs10456399
gnomAD v2: 6-31977789-A-G
gnomAD v3: 6-32010012-A-G
gnomAD v4: 6-32010012-A-G

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