Canonical Allele Identifier: CA45700710

Gene: TMEM178A

Linked Data

• dbSNP Id: rs760334853
• gnomAD v2: 2-39958982-T-C
• gnomAD v3: 2-39731842-T-C
• gnomAD v4: 2-39731842-T-C
• MyVariant Identifiers: chr2:g.39958982T>C (hg19) ; chr2:g.39731842T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39731842T>C , CM000664.2:g.39731842T>C	GRCh38
NC_000002.11:g.39958982T>C , CM000664.1:g.39958982T>C	GRCh37
NC_000002.10:g.39812486T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XM_024452702.1:c.401-3387T>C	XP_024308470.1:n.401-3387T>C