Canonical Allele Identifier: CA2831208498
Gene: TMEM178A HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
XM_024452702.1:c.401-3377G>T XP_024308470.1:n.401-3377G>T