Canonical Allele Identifier: CA45700718

Gene: TMEM178A

Linked Data

• dbSNP Id: rs989460501
• gnomAD v2: 2-39959001-G-C
• gnomAD v3: 2-39731861-G-C
• gnomAD v4: 2-39731861-G-C
• MyVariant Identifiers: chr2:g.39959001G>C (hg19) ; chr2:g.39731861G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39731861G>C , CM000664.2:g.39731861G>C	GRCh38
NC_000002.11:g.39959001G>C , CM000664.1:g.39959001G>C	GRCh37
NC_000002.10:g.39812505G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XM_024452702.1:c.401-3368G>C	XP_024308470.1:n.401-3368G>C