Canonical Allele Identifier: CA2749592466
Gene: TMEM178A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.39720526C>T , CM000664.2:g.39720526C>T GRCh38
NC_000002.11:g.39947666C>T , CM000664.1:g.39947666C>T GRCh37
NC_000002.10:g.39801170C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_024452702.1:c.401-14703C>T XP_024308470.1:n.401-14703C>T