Canonical Allele Identifier: CA2355680699
Gene: THBD HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23047762C= , CM000682.2:g.23047762C= GRCh38
NC_000020.10:g.23028399C= , CM000682.1:g.23028399C= GRCh37
NC_000020.9:g.22976399C= NCBI36
NG_012027.1:g.6903G= , LRG_168:g.6903G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000377103.3:c.*15G= MANE Select ENSP00000366307.2:n.*15G=
ENST00000377103.2:c.*15G= ENSP00000366307.2:n.*15G=
NM_000361.2:c.*15G= , LRG_168t1:c.*15G= NP_000352.1:n.*15G=
NM_000361.3:c.*15G= MANE Select NP_000352.1:n.*15G=
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