Canonical Allele Identifier: CA45700704

Gene: TMEM178A

Linked Data

• dbSNP Id: rs999390756
• gnomAD v2: 2-39958979-C-A
• gnomAD v3: 2-39731839-C-A
• gnomAD v4: 2-39731839-C-A
• MyVariant Identifiers: chr2:g.39958979C>A (hg19) ; chr2:g.39731839C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39731839C>A , CM000664.2:g.39731839C>A	GRCh38
NC_000002.11:g.39958979C>A , CM000664.1:g.39958979C>A	GRCh37
NC_000002.10:g.39812483C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XM_024452702.1:c.401-3390C>A	XP_024308470.1:n.401-3390C>A