Canonical Allele Identifier: CA11225133

Gene: TMEM178A

Linked Data

• dbSNP Id: rs10168666
• gnomAD v2: 2-39958971-C-T
• gnomAD v3: 2-39731831-C-T
• gnomAD v4: 2-39731831-C-T
• MyVariant Identifiers: chr2:g.39958971C>T (hg19) ; chr2:g.39731831C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39731831C>T , CM000664.2:g.39731831C>T	GRCh38
NC_000002.11:g.39958971C>T , CM000664.1:g.39958971C>T	GRCh37
NC_000002.10:g.39812475C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XM_024452702.1:c.401-3398C>T	XP_024308470.1:n.401-3398C>T