Canonical Allele Identifier: CA1029634388

Gene: TMEM178A

Linked Data

• dbSNP Id: rs1672925216
• gnomAD v3: 2-39731868-C-G
• gnomAD v4: 2-39731868-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39731868C>G , CM000664.2:g.39731868C>G	GRCh38
NC_000002.11:g.39959008C>G , CM000664.1:g.39959008C>G	GRCh37
NC_000002.10:g.39812512C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_024452702.1:c.401-3361C>G	XP_024308470.1:n.401-3361C>G