Canonical Allele Identifier: CA768621555

Gene: TMEM178A

Linked Data

• dbSNP Id: rs1300767396
• MyVariant Identifiers: chr2:g.39958965G>T (hg19) ; chr2:g.39731825G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39731825G>T , CM000664.2:g.39731825G>T	GRCh38
NC_000002.11:g.39958965G>T , CM000664.1:g.39958965G>T	GRCh37
NC_000002.10:g.39812469G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XM_024452702.1:c.401-3404G>T	XP_024308470.1:n.401-3404G>T