Canonical Allele Identifier: CA45700693

Gene: TMEM178A

Linked Data

• dbSNP Id: rs981079612
• gnomAD v2: 2-39958963-C-G
• gnomAD v3: 2-39731823-C-G
• gnomAD v4: 2-39731823-C-G
• MyVariant Identifiers: chr2:g.39958963C>G (hg19) ; chr2:g.39731823C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39731823C>G , CM000664.2:g.39731823C>G	GRCh38
NC_000002.11:g.39958963C>G , CM000664.1:g.39958963C>G	GRCh37
NC_000002.10:g.39812467C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XM_024452702.1:c.401-3406C>G	XP_024308470.1:n.401-3406C>G