Canonical Allele Identifier: CA408405447
Gene: THBD HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.23028668A>T (hg19) chr20:g.23048031A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23048031A>T , CM000682.2:g.23048031A>T GRCh38
NC_000020.10:g.23028668A>T , CM000682.1:g.23028668A>T GRCh37
NC_000020.9:g.22976668A>T NCBI36
NG_012027.1:g.6634T>A , LRG_168:g.6634T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000377103.3:c.1474T>A MANE Select ENSP00000366307.2:p.Ser492Thr
ENST00000377103.2:c.1474T>A ENSP00000366307.2:p.Ser492Thr
NM_000361.2:c.1474T>A , LRG_168t1:c.1474T>A NP_000352.1:p.Ser492Thr
NM_000361.3:c.1474T>A MANE Select NP_000352.1:p.Ser492Thr
Search 100 bp 5'
Search 100 bp 3'