Canonical Allele Identifier: CA1246500900
Gene: TMEM178A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.39731855C= , CM000664.2:g.39731855C= GRCh38
NC_000002.11:g.39958995C= , CM000664.1:g.39958995C= GRCh37
NC_000002.10:g.39812499C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_024452702.1:c.401-3374C= XP_024308470.1:n.401-3374C=