Canonical Allele Identifier: CA2355680755
Gene: THBD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23047833A= , CM000682.2:g.23047833A= GRCh38
NC_000020.10:g.23028470A= , CM000682.1:g.23028470A= GRCh37
NC_000020.9:g.22976470A= NCBI36
NG_012027.1:g.6832T= , LRG_168:g.6832T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000377103.3:c.1672T= MANE Select ENSP00000366307.2:p.Ser558=
ENST00000377103.2:c.1672T= ENSP00000366307.2:p.Ser558=
NM_000361.2:c.1672T= , LRG_168t1:c.1672T= NP_000352.1:p.Ser558=
NM_000361.3:c.1672T= MANE Select NP_000352.1:p.Ser558=