Canonical Allele Identifier: CA2355681552
Gene: THBD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23049389T= , CM000682.2:g.23049389T= GRCh38
NC_000020.10:g.23030026T= , CM000682.1:g.23030026T= GRCh37
NC_000020.9:g.22978026T= NCBI36
NG_012027.1:g.5276A= , LRG_168:g.5276A=

Transcript Alleles

HGVS Amino-acid change
ENST00000377103.3:c.116A= MANE Select ENSP00000366307.2:p.Tyr39=
ENST00000377103.2:c.116A= ENSP00000366307.2:p.Tyr39=
NM_000361.2:c.116A= , LRG_168t1:c.116A= NP_000352.1:p.Tyr39=
NM_000361.3:c.116A= MANE Select NP_000352.1:p.Tyr39=