Canonical Allele Identifier: CA45700770

Gene: TMEM178A

Linked Data

• dbSNP Id: rs546244628
• gnomAD v2: 2-39959100-T-C
• gnomAD v3: 2-39731960-T-C
• gnomAD v4: 2-39731960-T-C
• MyVariant Identifiers: chr2:g.39959100T>C (hg19) ; chr2:g.39731960T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39731960T>C , CM000664.2:g.39731960T>C	GRCh38
NC_000002.11:g.39959100T>C , CM000664.1:g.39959100T>C	GRCh37
NC_000002.10:g.39812604T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XM_024452702.1:c.401-3269T>C	XP_024308470.1:n.401-3269T>C