Canonical Allele Identifier: CA1246495274
Gene: TMEM178A HGNC NCBI

Linked Data

dbSNP Id: rs1672682061
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.39720531C>T , CM000664.2:g.39720531C>T GRCh38
NC_000002.11:g.39947671C>T , CM000664.1:g.39947671C>T GRCh37
NC_000002.10:g.39801175C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_024452702.1:c.401-14698C>T XP_024308470.1:n.401-14698C>T
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