Canonical Allele Identifier: CA2372589115

Gene: PRELID3B

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.59038947A= , CM000682.2:g.59038947A=	GRCh38
NC_000020.10:g.57614002A= , CM000682.1:g.57614002A=	GRCh37
NC_000020.9:g.57047397A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_016045.3:c.33-313T= MANE Select	NP_057129.2:n.33-313T=
ENST00000355937.9:c.33-313T= MANE Select	ENSP00000348206.4:n.33-313T=
NM_001256403.1:c.33-313T=	NP_001243332.1:n.33-313T=
NM_001256403.2:c.33-313T=	NP_001243332.1:n.33-313T=
NM_016045.2:c.33-313T=	NP_057129.2:n.33-313T=
NR_037929.1:n.149-313T=
NR_037930.1:n.149-2187T=
ENST00000355937.8:c.33-313T=	ENSP00000348206.4:n.33-313T=
ENST00000371033.9:c.33-313T=	ENSP00000360072.5:n.33-313T=
ENST00000463057.1:c.33-313T=	ENSP00000431440.1:n.33-313T=
ENST00000466051.1:n.112-313T=