Canonical Allele Identifier: CA1246500948
Gene: TMEM178A HGNC NCBI

Linked Data

dbSNP Id: rs1672928428

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.39731933_39731942del , CM000664.2:g.39731933_39731942del GRCh38
NC_000002.11:g.39959073_39959082del , CM000664.1:g.39959073_39959082del GRCh37
NC_000002.10:g.39812577_39812586del NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_024452702.1:c.401-3296_401-3287del XP_024308470.1:n.401-3296_401-3287del