Canonical Allele Identifier: CA2355680854
Gene: THBD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23048011G= , CM000682.2:g.23048011G= GRCh38
NC_000020.10:g.23028648G= , CM000682.1:g.23028648G= GRCh37
NC_000020.9:g.22976648G= NCBI36
NG_012027.1:g.6654C= , LRG_168:g.6654C=

Transcript Alleles

HGVS Amino-acid change
ENST00000377103.3:c.1494C= MANE Select ENSP00000366307.2:p.Ser498=
ENST00000377103.2:c.1494C= ENSP00000366307.2:p.Ser498=
NM_000361.2:c.1494C= , LRG_168t1:c.1494C= NP_000352.1:p.Ser498=
NM_000361.3:c.1494C= MANE Select NP_000352.1:p.Ser498=