Canonical Allele Identifier: CA1562059712
Gene: TMEM161B-DT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.88367793C= , CM000667.2:g.88367793C= GRCh38
NC_000005.9:g.87663610C= , CM000667.1:g.87663610C= GRCh37
NC_000005.8:g.87699366C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_039993.1:n.207-42280C=
NR_039994.2:n.165-42280C=
NR_039995.1:n.207-68480C=
NR_105019.1:n.586-42280C=