Canonical Allele Identifier: CA2355679987
Gene: THBD HGNC NCBI

Linked Data

dbSNP Id: rs1984566640
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23046221A>G , CM000682.2:g.23046221A>G GRCh38
NC_000020.10:g.23026858A>G , CM000682.1:g.23026858A>G GRCh37
NC_000020.9:g.22974858A>G NCBI36
NG_012027.1:g.8444T>C , LRG_168:g.8444T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000377103.3:c.*1556T>C MANE Select ENSP00000366307.2:n.*1556T>C
ENST00000377103.2:c.*1556T>C ENSP00000366307.2:n.*1556T>C
NM_000361.2:c.*1556T>C , LRG_168t1:c.*1556T>C NP_000352.1:n.*1556T>C
NM_000361.3:c.*1556T>C MANE Select NP_000352.1:n.*1556T>C
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