Canonical Allele Identifier: CA1246500898
Gene: TMEM178A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.39731852G= , CM000664.2:g.39731852G= GRCh38
NC_000002.11:g.39958992G= , CM000664.1:g.39958992G= GRCh37
NC_000002.10:g.39812496G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_024452702.1:c.401-3377G= XP_024308470.1:n.401-3377G=