Canonical Allele Identifier: CA408405068
Gene: THBD HGNC NCBI

Linked Data

dbSNP Id: rs1425074549

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23047845A>C , CM000682.2:g.23047845A>C GRCh38
NC_000020.10:g.23028482A>C , CM000682.1:g.23028482A>C GRCh37
NC_000020.9:g.22976482A>C NCBI36
NG_012027.1:g.6820T>G , LRG_168:g.6820T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000377103.3:c.1660T>G MANE Select ENSP00000366307.2:p.Cys554Gly
ENST00000377103.2:c.1660T>G ENSP00000366307.2:p.Cys554Gly
NM_000361.2:c.1660T>G , LRG_168t1:c.1660T>G NP_000352.1:p.Cys554Gly
NM_000361.3:c.1660T>G MANE Select NP_000352.1:p.Cys554Gly