Canonical Allele Identifier: CA2581765073
Gene: TMEM178A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.39731920A>T , CM000664.2:g.39731920A>T GRCh38
NC_000002.11:g.39959060A>T , CM000664.1:g.39959060A>T GRCh37
NC_000002.10:g.39812564A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_024452702.1:c.401-3309A>T XP_024308470.1:n.401-3309A>T