Canonical Allele Identifier: CA531981575
Gene: TMEM178A HGNC NCBI

Linked Data

dbSNP Id: rs1442626507
gnomAD v2: 2-39959134-G-A
gnomAD v3: 2-39731994-G-A
gnomAD v4: 2-39731994-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.39731994G>A , CM000664.2:g.39731994G>A GRCh38
NC_000002.11:g.39959134G>A , CM000664.1:g.39959134G>A GRCh37
NC_000002.10:g.39812638G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_024452702.1:c.401-3235G>A XP_024308470.1:n.401-3235G>A