Canonical Allele Identifier: CA45700650
Gene: TMEM178A HGNC NCBI

Linked Data

dbSNP Id: rs972766314
gnomAD v2: 2-39958923-C-T
gnomAD v3: 2-39731783-C-T
gnomAD v4: 2-39731783-C-T
MyVariant Identifiers: chr2:g.39958923C>T (hg19) chr2:g.39731783C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.39731783C>T , CM000664.2:g.39731783C>T GRCh38
NC_000002.11:g.39958923C>T , CM000664.1:g.39958923C>T GRCh37
NC_000002.10:g.39812427C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_024452702.1:c.401-3446C>T XP_024308470.1:n.401-3446C>T
Search 100 bp 5'
Search 100 bp 3'