Canonical Allele Identifier: CA408405128
Gene: THBD HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.23028508G>T (hg19) chr20:g.23047871G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23047871G>T , CM000682.2:g.23047871G>T GRCh38
NC_000020.10:g.23028508G>T , CM000682.1:g.23028508G>T GRCh37
NC_000020.9:g.22976508G>T NCBI36
NG_012027.1:g.6794C>A , LRG_168:g.6794C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000377103.3:c.1634C>A MANE Select ENSP00000366307.2:p.Ala545Asp
ENST00000377103.2:c.1634C>A ENSP00000366307.2:p.Ala545Asp
NM_000361.2:c.1634C>A , LRG_168t1:c.1634C>A NP_000352.1:p.Ala545Asp
NM_000361.3:c.1634C>A MANE Select NP_000352.1:p.Ala545Asp
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