Canonical Allele Identifier: CA313550194
Gene: THBD HGNC NCBI

Linked Data

ClinVar Variation Id: 1310038
ClinVar RCV Id: RCV001757106
dbSNP Id: rs865948837
gnomAD v4: 20-23047800-C-G
MyVariant Identifiers: chr20:g.23028437C>G (hg19) chr20:g.23047800C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23047800C>G , CM000682.2:g.23047800C>G GRCh38
NC_000020.10:g.23028437C>G , CM000682.1:g.23028437C>G GRCh37
NC_000020.9:g.22976437C>G NCBI36
NG_012027.1:g.6865G>C , LRG_168:g.6865G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000377103.3:c.1705G>C MANE Select ENSP00000366307.2:p.Glu569Gln
ENST00000377103.2:c.1705G>C ENSP00000366307.2:p.Glu569Gln
NM_000361.2:c.1705G>C , LRG_168t1:c.1705G>C NP_000352.1:p.Glu569Gln
NM_000361.3:c.1705G>C MANE Select NP_000352.1:p.Glu569Gln
Search 100 bp 5'
Search 100 bp 3'