Canonical Allele Identifier: CA531981558
Gene: TMEM178A HGNC NCBI

Linked Data

dbSNP Id: rs1483120208
gnomAD v2: 2-39959021-G-A
gnomAD v3: 2-39731881-G-A
gnomAD v4: 2-39731881-G-A
MyVariant Identifiers: chr2:g.39959021G>A (hg19) chr2:g.39731881G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.39731881G>A , CM000664.2:g.39731881G>A GRCh38
NC_000002.11:g.39959021G>A , CM000664.1:g.39959021G>A GRCh37
NC_000002.10:g.39812525G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_024452702.1:c.401-3348G>A XP_024308470.1:n.401-3348G>A
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