Canonical Allele Identifier: CA1029634378
Gene: TMEM178A HGNC NCBI

Linked Data

dbSNP Id: rs1672924620
gnomAD v3: 2-39731833-C-G
gnomAD v4: 2-39731833-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.39731833C>G , CM000664.2:g.39731833C>G GRCh38
NC_000002.11:g.39958973C>G , CM000664.1:g.39958973C>G GRCh37
NC_000002.10:g.39812477C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_024452702.1:c.401-3396C>G XP_024308470.1:n.401-3396C>G