Canonical Allele Identifier: CA2749592712

Gene: TMEM178A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39731866C>A , CM000664.2:g.39731866C>A	GRCh38
NC_000002.11:g.39959006C>A , CM000664.1:g.39959006C>A	GRCh37
NC_000002.10:g.39812510C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XM_024452702.1:c.401-3363C>A	XP_024308470.1:n.401-3363C>A