Canonical Allele Identifier: CA45700804
Gene: TMEM178A HGNC NCBI

Linked Data

dbSNP Id: rs1006112968
gnomAD v3: 2-39731993-G-C
gnomAD v4: 2-39731993-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.39731993G>C , CM000664.2:g.39731993G>C GRCh38
NC_000002.11:g.39959133G>C , CM000664.1:g.39959133G>C GRCh37
NC_000002.10:g.39812637G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_024452702.1:c.401-3236G>C XP_024308470.1:n.401-3236G>C