Canonical Allele Identifier: CA1246500901
Gene: TMEM178A HGNC NCBI

Linked Data

dbSNP Id: rs1672925041

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.39731855C>T , CM000664.2:g.39731855C>T GRCh38
NC_000002.11:g.39958995C>T , CM000664.1:g.39958995C>T GRCh37
NC_000002.10:g.39812499C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_024452702.1:c.401-3374C>T XP_024308470.1:n.401-3374C>T