Canonical Allele Identifier: CA2355680749
Gene: THBD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23047822T= , CM000682.2:g.23047822T= GRCh38
NC_000020.10:g.23028459T= , CM000682.1:g.23028459T= GRCh37
NC_000020.9:g.22976459T= NCBI36
NG_012027.1:g.6843A= , LRG_168:g.6843A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000377103.3:c.1683A= MANE Select ENSP00000366307.2:p.Val561=
ENST00000377103.2:c.1683A= ENSP00000366307.2:p.Val561=
NM_000361.2:c.1683A= , LRG_168t1:c.1683A= NP_000352.1:p.Val561=
NM_000361.3:c.1683A= MANE Select NP_000352.1:p.Val561=