Canonical Allele Identifier: CA408405090
Gene: THBD HGNC NCBI

Linked Data

dbSNP Id: rs1268675176
gnomAD v3: 20-23047853-T-A
gnomAD v4: 20-23047853-T-A
MyVariant Identifiers: chr20:g.23028490T>A (hg19) chr20:g.23047853T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23047853T>A , CM000682.2:g.23047853T>A GRCh38
NC_000020.10:g.23028490T>A , CM000682.1:g.23028490T>A GRCh37
NC_000020.9:g.22976490T>A NCBI36
NG_012027.1:g.6812A>T , LRG_168:g.6812A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000377103.3:c.1652A>T MANE Select ENSP00000366307.2:p.Glu551Val
ENST00000377103.2:c.1652A>T ENSP00000366307.2:p.Glu551Val
NM_000361.2:c.1652A>T , LRG_168t1:c.1652A>T NP_000352.1:p.Glu551Val
NM_000361.3:c.1652A>T MANE Select NP_000352.1:p.Glu551Val
Search 100 bp 5'
Search 100 bp 3'