Canonical Allele Identifier: CA2355680739
Gene: THBD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23047808A= , CM000682.2:g.23047808A= GRCh38
NC_000020.10:g.23028445A= , CM000682.1:g.23028445A= GRCh37
NC_000020.9:g.22976445A= NCBI36
NG_012027.1:g.6857T= , LRG_168:g.6857T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000377103.3:c.1697T= MANE Select ENSP00000366307.2:p.Val566=
ENST00000377103.2:c.1697T= ENSP00000366307.2:p.Val566=
NM_000361.2:c.1697T= , LRG_168t1:c.1697T= NP_000352.1:p.Val566=
NM_000361.3:c.1697T= MANE Select NP_000352.1:p.Val566=