Canonical Allele Identifier: CA2355681644
Gene: THBD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23049555A= , CM000682.2:g.23049555A= GRCh38
NC_000020.10:g.23030192A= , CM000682.1:g.23030192A= GRCh37
NC_000020.9:g.22978192A= NCBI36
NG_012027.1:g.5110T= , LRG_168:g.5110T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000377103.3:c.-51T= MANE Select ENSP00000366307.2:n.-51T=
ENST00000377103.2:c.-51T= ENSP00000366307.2:n.-51T=
NM_000361.2:c.-51T= , LRG_168t1:c.-51T= NP_000352.1:n.-51T=
NM_000361.3:c.-51T= MANE Select NP_000352.1:n.-51T=