Canonical Allele Identifier: CA2448303091

Gene: HNRNPH2 RPL36A-HNRNPH2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101412795A= , CM000685.2:g.101412795A=	GRCh38
NC_000023.10:g.100667783A= , CM000685.1:g.100667783A=	GRCh37
NC_000023.9:g.100554439A=	NCBI36
NG_007119.1:g.169T= , LRG_672:g.169T=
NG_016327.1:g.9593A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316594.6:c.807A= (HNRNPH2) MANE Select	ENSP00000361927.2:p.Ser269=
ENST00000316594.5:c.807A= (HNRNPH2)	ENSP00000361927.2:p.Ser269=
NM_001032393.2:c.807A= (HNRNPH2)	NP_001027565.1:p.Ser269=
NM_001199973.1:c.*803A= (RPL36A-HNRNPH2)	NP_001186902.1:n.*803A=
NM_001199974.1:c.*803A= (RPL36A-HNRNPH2)	NP_001186903.1:n.*803A=
NM_019597.4:c.807A= (HNRNPH2)	NP_062543.1:p.Ser269=
NM_001199973.2:c.*803A= (RPL36A-HNRNPH2)	NP_001186902.2:n.*803A=
NM_001199974.2:c.*803A= (RPL36A-HNRNPH2)	NP_001186903.2:n.*803A=
NM_019597.5:c.807A= (HNRNPH2) MANE Select	NP_062543.1:p.Ser269=
NM_001032393.3:c.807A= (HNRNPH2)	NP_001027565.1:p.Ser269=