Canonical Allele Identifier: CA45700707

Gene: TMEM178A

Linked Data

• dbSNP Id: rs1031991955
• MyVariant Identifiers: chr2:g.39958980C>T (hg19) ; chr2:g.39731840C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39731840C>T , CM000664.2:g.39731840C>T	GRCh38
NC_000002.11:g.39958980C>T , CM000664.1:g.39958980C>T	GRCh37
NC_000002.10:g.39812484C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XM_024452702.1:c.401-3389C>T	XP_024308470.1:n.401-3389C>T