Canonical Allele Identifier: CA2355680869

Gene: THBD

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.23048034C= , CM000682.2:g.23048034C=	GRCh38
NC_000020.10:g.23028671C= , CM000682.1:g.23028671C=	GRCh37
NC_000020.9:g.22976671C=	NCBI36
NG_012027.1:g.6631G= , LRG_168:g.6631G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377103.3:c.1471G= MANE Select	ENSP00000366307.2:p.Gly491=
ENST00000377103.2:c.1471G=	ENSP00000366307.2:p.Gly491=
NM_000361.2:c.1471G= , LRG_168t1:c.1471G=	NP_000352.1:p.Gly491=
NM_000361.3:c.1471G= MANE Select	NP_000352.1:p.Gly491=