Canonical Allele Identifier: CA2699346706
Gene: TMEM178A HGNC NCBI

Linked Data

dbSNP Id: rs2148130527

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.39731864A>C , CM000664.2:g.39731864A>C GRCh38
NC_000002.11:g.39959004A>C , CM000664.1:g.39959004A>C GRCh37
NC_000002.10:g.39812508A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_024452702.1:c.401-3365A>C XP_024308470.1:n.401-3365A>C