Canonical Allele Identifier: CA1246500919
Gene: TMEM178A HGNC NCBI

Linked Data

dbSNP Id: rs1672925418

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.39731882G>A , CM000664.2:g.39731882G>A GRCh38
NC_000002.11:g.39959022G>A , CM000664.1:g.39959022G>A GRCh37
NC_000002.10:g.39812526G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_024452702.1:c.401-3347G>A XP_024308470.1:n.401-3347G>A