Canonical Allele Identifier: CA1246500882
Gene: TMEM178A HGNC NCBI

Linked Data

dbSNP Id: rs1572708498

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.39731824T>G , CM000664.2:g.39731824T>G GRCh38
NC_000002.11:g.39958964T>G , CM000664.1:g.39958964T>G GRCh37
NC_000002.10:g.39812468T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_024452702.1:c.401-3405T>G XP_024308470.1:n.401-3405T>G