Canonical Allele Identifier: CA2355680769

Gene: THBD

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.23047850T= , CM000682.2:g.23047850T=	GRCh38
NC_000020.10:g.23028487T= , CM000682.1:g.23028487T=	GRCh37
NC_000020.9:g.22976487T=	NCBI36
NG_012027.1:g.6815A= , LRG_168:g.6815A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377103.3:c.1655A= MANE Select	ENSP00000366307.2:p.Tyr552=
ENST00000377103.2:c.1655A=	ENSP00000366307.2:p.Tyr552=
NM_000361.2:c.1655A= , LRG_168t1:c.1655A=	NP_000352.1:p.Tyr552=
NM_000361.3:c.1655A= MANE Select	NP_000352.1:p.Tyr552=