Canonical Allele Identifier: CA1246495268
Gene: TMEM178A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.39720519A= , CM000664.2:g.39720519A= GRCh38
NC_000002.11:g.39947659A= , CM000664.1:g.39947659A= GRCh37
NC_000002.10:g.39801163A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_024452702.1:c.401-14710A= XP_024308470.1:n.401-14710A=