Canonical Allele Identifier: CA2355681497
Gene: THBD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23049287A= , CM000682.2:g.23049287A= GRCh38
NC_000020.10:g.23029924A= , CM000682.1:g.23029924A= GRCh37
NC_000020.9:g.22977924A= NCBI36
NG_012027.1:g.5378T= , LRG_168:g.5378T=

Transcript Alleles

HGVS Amino-acid change
ENST00000377103.3:c.218T= MANE Select ENSP00000366307.2:p.Leu73=
ENST00000377103.2:c.218T= ENSP00000366307.2:p.Leu73=
NM_000361.2:c.218T= , LRG_168t1:c.218T= NP_000352.1:p.Leu73=
NM_000361.3:c.218T= MANE Select NP_000352.1:p.Leu73=