Canonical Allele Identifier: CA449694495

Gene: TNXA

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32009614C>G , CM000668.2:g.32009614C>G	GRCh38
NC_000006.11:g.31977391C>G , CM000668.1:g.31977391C>G	GRCh37
NC_000006.10:g.32085369C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000507684.1:n.1527G>C
NR_001284.2:n.2078G>C