Canonical Allele Identifier: CA2355680761

Gene: THBD

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.23047839C= , CM000682.2:g.23047839C=	GRCh38
NC_000020.10:g.23028476C= , CM000682.1:g.23028476C=	GRCh37
NC_000020.9:g.22976476C=	NCBI36
NG_012027.1:g.6826G= , LRG_168:g.6826G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377103.3:c.1666G= MANE Select	ENSP00000366307.2:p.Ala556=
ENST00000377103.2:c.1666G=	ENSP00000366307.2:p.Ala556=
NM_000361.2:c.1666G= , LRG_168t1:c.1666G=	NP_000352.1:p.Ala556=
NM_000361.3:c.1666G= MANE Select	NP_000352.1:p.Ala556=