Canonical Allele Identifier: CA45700685

Gene: TMEM178A

Linked Data

• dbSNP Id: rs971299403
• gnomAD v2: 2-39958961-TTCTG-T
• gnomAD v3: 2-39731821-TTCTG-T
• gnomAD v4: 2-39731821-TTCTG-T
• MyVariant Identifiers: chr2:g.39958962_39958965del (hg19) ; chr2:g.39731822_39731825del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39731829_39731832del , CM000664.2:g.39731829_39731832del	GRCh38
NC_000002.11:g.39958969_39958972del , CM000664.1:g.39958969_39958972del	GRCh37
NC_000002.10:g.39812473_39812476del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XM_024452702.1:c.401-3400_401-3397del	XP_024308470.1:n.401-3400_401-3397del