Canonical Allele Identifier: CA408404969
Gene: THBD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23047794T>A , CM000682.2:g.23047794T>A GRCh38
NC_000020.10:g.23028431T>A , CM000682.1:g.23028431T>A GRCh37
NC_000020.9:g.22976431T>A NCBI36
NG_012027.1:g.6871A>T , LRG_168:g.6871A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000377103.3:c.1711A>T MANE Select ENSP00000366307.2:p.Thr571Ser
ENST00000377103.2:c.1711A>T ENSP00000366307.2:p.Thr571Ser
NM_000361.2:c.1711A>T , LRG_168t1:c.1711A>T NP_000352.1:p.Thr571Ser
NM_000361.3:c.1711A>T MANE Select NP_000352.1:p.Thr571Ser