Canonical Allele Identifier: CA2652141734
Gene: THBD HGNC NCBI

Linked Data

gnomAD v4: 20-23049556-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23049556C>T , CM000682.2:g.23049556C>T GRCh38
NC_000020.10:g.23030193C>T , CM000682.1:g.23030193C>T GRCh37
NC_000020.9:g.22978193C>T NCBI36
NG_012027.1:g.5109G>A , LRG_168:g.5109G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000377103.3:c.-52G>A MANE Select ENSP00000366307.2:n.-52G>A
ENST00000377103.2:c.-52G>A ENSP00000366307.2:n.-52G>A
NM_000361.2:c.-52G>A , LRG_168t1:c.-52G>A NP_000352.1:n.-52G>A
NM_000361.3:c.-52G>A MANE Select NP_000352.1:n.-52G>A
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