Canonical Allele Identifier: CA2355681647

Gene: THBD

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.23049562C= , CM000682.2:g.23049562C=	GRCh38
NC_000020.10:g.23030199C= , CM000682.1:g.23030199C=	GRCh37
NC_000020.9:g.22978199C=	NCBI36
NG_012027.1:g.5103G= , LRG_168:g.5103G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000377103.3:c.-58G= MANE Select	ENSP00000366307.2:n.-58G=
ENST00000377103.2:c.-58G=	ENSP00000366307.2:n.-58G=
NM_000361.2:c.-58G= , LRG_168t1:c.-58G=	NP_000352.1:n.-58G=
NM_000361.3:c.-58G= MANE Select	NP_000352.1:n.-58G=