Canonical Allele Identifier: CA2355680664

Gene: THBD

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.23047706C= , CM000682.2:g.23047706C=	GRCh38
NC_000020.10:g.23028343C= , CM000682.1:g.23028343C=	GRCh37
NC_000020.9:g.22976343C=	NCBI36
NG_012027.1:g.6959G= , LRG_168:g.6959G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377103.3:c.*71G= MANE Select	ENSP00000366307.2:n.*71G=
ENST00000377103.2:c.*71G=	ENSP00000366307.2:n.*71G=
NM_000361.2:c.*71G= , LRG_168t1:c.*71G=	NP_000352.1:n.*71G=
NM_000361.3:c.*71G= MANE Select	NP_000352.1:n.*71G=