Canonical Allele Identifier: CA2355680668

Gene: THBD

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.23047715C= , CM000682.2:g.23047715C=	GRCh38
NC_000020.10:g.23028352C= , CM000682.1:g.23028352C=	GRCh37
NC_000020.9:g.22976352C=	NCBI36
NG_012027.1:g.6950G= , LRG_168:g.6950G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377103.3:c.*62G= MANE Select	ENSP00000366307.2:n.*62G=
ENST00000377103.2:c.*62G=	ENSP00000366307.2:n.*62G=
NM_000361.2:c.*62G= , LRG_168t1:c.*62G=	NP_000352.1:n.*62G=
NM_000361.3:c.*62G= MANE Select	NP_000352.1:n.*62G=