Canonical Allele Identifier: CA2355680865

Gene: THBD

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.23048027C= , CM000682.2:g.23048027C=	GRCh38
NC_000020.10:g.23028664C= , CM000682.1:g.23028664C=	GRCh37
NC_000020.9:g.22976664C=	NCBI36
NG_012027.1:g.6638G= , LRG_168:g.6638G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377103.3:c.1478G= MANE Select	ENSP00000366307.2:p.Gly493=
ENST00000377103.2:c.1478G=	ENSP00000366307.2:p.Gly493=
NM_000361.2:c.1478G= , LRG_168t1:c.1478G=	NP_000352.1:p.Gly493=
NM_000361.3:c.1478G= MANE Select	NP_000352.1:p.Gly493=