Canonical Allele Identifier: CA2355680747
Gene: THBD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23047820A= , CM000682.2:g.23047820A= GRCh38
NC_000020.10:g.23028457A= , CM000682.1:g.23028457A= GRCh37
NC_000020.9:g.22976457A= NCBI36
NG_012027.1:g.6845T= , LRG_168:g.6845T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000377103.3:c.1685T= MANE Select ENSP00000366307.2:p.Val562=
ENST00000377103.2:c.1685T= ENSP00000366307.2:p.Val562=
NM_000361.2:c.1685T= , LRG_168t1:c.1685T= NP_000352.1:p.Val562=
NM_000361.3:c.1685T= MANE Select NP_000352.1:p.Val562=