Canonical Allele Identifier: CA1246500830
Gene: TMEM178A HGNC NCBI

Linked Data

dbSNP Id: rs1672922444
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.39731733C>T , CM000664.2:g.39731733C>T GRCh38
NC_000002.11:g.39958873C>T , CM000664.1:g.39958873C>T GRCh37
NC_000002.10:g.39812377C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_024452702.1:c.401-3496C>T XP_024308470.1:n.401-3496C>T
Search 100 bp 5'
Search 100 bp 3'