Canonical Allele Identifier: CA2355680763
Gene: THBD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23047842C= , CM000682.2:g.23047842C= GRCh38
NC_000020.10:g.23028479C= , CM000682.1:g.23028479C= GRCh37
NC_000020.9:g.22976479C= NCBI36
NG_012027.1:g.6823G= , LRG_168:g.6823G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000377103.3:c.1663G= MANE Select ENSP00000366307.2:p.Ala555=
ENST00000377103.2:c.1663G= ENSP00000366307.2:p.Ala555=
NM_000361.2:c.1663G= , LRG_168t1:c.1663G= NP_000352.1:p.Ala555=
NM_000361.3:c.1663G= MANE Select NP_000352.1:p.Ala555=