Canonical Allele Identifier: CA2503665207
Gene: TMEM178A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.39731725T>A , CM000664.2:g.39731725T>A GRCh38
NC_000002.11:g.39958865T>A , CM000664.1:g.39958865T>A GRCh37
NC_000002.10:g.39812369T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_024452702.1:c.401-3504T>A XP_024308470.1:n.401-3504T>A