Canonical Allele Identifier: CA2355681596
Gene: THBD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23049476A= , CM000682.2:g.23049476A= GRCh38
NC_000020.10:g.23030113A= , CM000682.1:g.23030113A= GRCh37
NC_000020.9:g.22978113A= NCBI36
NG_012027.1:g.5189T= , LRG_168:g.5189T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000377103.3:c.29T= MANE Select ENSP00000366307.2:p.Leu10=
ENST00000377103.2:c.29T= ENSP00000366307.2:p.Leu10=
NM_000361.2:c.29T= , LRG_168t1:c.29T= NP_000352.1:p.Leu10=
NM_000361.3:c.29T= MANE Select NP_000352.1:p.Leu10=