Canonical Allele Identifier: CA635265760
Gene: THBD HGNC NCBI

Linked Data

dbSNP Id: rs1390746246
gnomAD v2: 20-23028393-A-T
gnomAD v4: 20-23047756-A-T
MyVariant Identifiers: chr20:g.23028393A>T (hg19) chr20:g.23047756A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23047756A>T , CM000682.2:g.23047756A>T GRCh38
NC_000020.10:g.23028393A>T , CM000682.1:g.23028393A>T GRCh37
NC_000020.9:g.22976393A>T NCBI36
NG_012027.1:g.6909T>A , LRG_168:g.6909T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000377103.3:c.*21T>A MANE Select ENSP00000366307.2:n.*21T>A
ENST00000377103.2:c.*21T>A ENSP00000366307.2:n.*21T>A
NM_000361.2:c.*21T>A , LRG_168t1:c.*21T>A NP_000352.1:n.*21T>A
NM_000361.3:c.*21T>A MANE Select NP_000352.1:n.*21T>A
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