Canonical Allele Identifier: CA510161162
Gene: THBD HGNC NCBI

Linked Data

gnomAD v4: 20-23049382-G-A
MyVariant Identifiers: chr20:g.23030019G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23049382G>A , CM000682.2:g.23049382G>A GRCh38
NC_000020.10:g.23030019G>A , CM000682.1:g.23030019G>A GRCh37
NC_000020.9:g.22978019G>A NCBI36
NG_012027.1:g.5283C>T , LRG_168:g.5283C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000377103.3:c.123C>T MANE Select ENSP00000366307.2:p.Gly41=
ENST00000377103.2:c.123C>T ENSP00000366307.2:p.Gly41=
NM_000361.2:c.123C>T , LRG_168t1:c.123C>T NP_000352.1:p.Gly41=
NM_000361.3:c.123C>T MANE Select NP_000352.1:p.Gly41=
Search 100 bp 5'
Search 100 bp 3'