Canonical Allele Identifier: CA408408332
Gene: THBD HGNC NCBI

Linked Data

gnomAD v4: 20-23049383-C-A
MyVariant Identifiers: chr20:g.23030020C>A (hg19) chr20:g.23049383C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23049383C>A , CM000682.2:g.23049383C>A GRCh38
NC_000020.10:g.23030020C>A , CM000682.1:g.23030020C>A GRCh37
NC_000020.9:g.22978020C>A NCBI36
NG_012027.1:g.5282G>T , LRG_168:g.5282G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000377103.3:c.122G>T MANE Select ENSP00000366307.2:p.Gly41Val
ENST00000377103.2:c.122G>T ENSP00000366307.2:p.Gly41Val
NM_000361.2:c.122G>T , LRG_168t1:c.122G>T NP_000352.1:p.Gly41Val
NM_000361.3:c.122G>T MANE Select NP_000352.1:p.Gly41Val
Search 100 bp 5'
Search 100 bp 3'