Canonical Allele Identifier: CA2231570270
Gene: TXNL4B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.72080103C>A , CM000678.2:g.72080103C>A GRCh38
NC_000016.9:g.72114002C>A , CM000678.1:g.72114002C>A GRCh37
NC_000016.8:g.70671503C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000562153.5:c.284+8884G>T ENSP00000454635.1:n.284+8884G>T
XM_017023377.2:c.284+8884G>T XP_016878866.1:n.284+8884G>T