Canonical Allele Identifier: CA1029634370
Gene: TMEM178A HGNC NCBI

Linked Data

dbSNP Id: rs1672924176
gnomAD v3: 2-39731808-G-T
gnomAD v4: 2-39731808-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.39731808G>T , CM000664.2:g.39731808G>T GRCh38
NC_000002.11:g.39958948G>T , CM000664.1:g.39958948G>T GRCh37
NC_000002.10:g.39812452G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_024452702.1:c.401-3421G>T XP_024308470.1:n.401-3421G>T
Search 100 bp 5'
Search 100 bp 3'