Canonical Allele Identifier: CA2355681591

Gene: THBD

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.23049466G= , CM000682.2:g.23049466G=	GRCh38
NC_000020.10:g.23030103G= , CM000682.1:g.23030103G=	GRCh37
NC_000020.9:g.22978103G=	NCBI36
NG_012027.1:g.5199C= , LRG_168:g.5199C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377103.3:c.39C= MANE Select	ENSP00000366307.2:p.Ala13=
ENST00000377103.2:c.39C=	ENSP00000366307.2:p.Ala13=
NM_000361.2:c.39C= , LRG_168t1:c.39C=	NP_000352.1:p.Ala13=
NM_000361.3:c.39C= MANE Select	NP_000352.1:p.Ala13=