Canonical Allele Identifier: CA45700737
Gene: TMEM178A HGNC NCBI

Linked Data

dbSNP Id: rs954571133
gnomAD v3: 2-39731897-T-C
gnomAD v4: 2-39731897-T-C
MyVariant Identifiers: chr2:g.39959037T>C (hg19) chr2:g.39731897T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.39731897T>C , CM000664.2:g.39731897T>C GRCh38
NC_000002.11:g.39959037T>C , CM000664.1:g.39959037T>C GRCh37
NC_000002.10:g.39812541T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_024452702.1:c.401-3332T>C XP_024308470.1:n.401-3332T>C
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