Canonical Allele Identifier: CA2448303050

Gene: HNRNPH2 RPL36A-HNRNPH2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101412614C= , CM000685.2:g.101412614C=	GRCh38
NC_000023.10:g.100667602C= , CM000685.1:g.100667602C=	GRCh37
NC_000023.9:g.100554258C=	NCBI36
NG_007119.1:g.350G= , LRG_672:g.350G=
NG_016327.1:g.9412C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316594.6:c.626C= (HNRNPH2) MANE Select	ENSP00000361927.2:p.Pro209=
ENST00000316594.5:c.626C= (HNRNPH2)	ENSP00000361927.2:p.Pro209=
NM_001032393.2:c.626C= (HNRNPH2)	NP_001027565.1:p.Pro209=
NM_001199973.1:c.*622C= (RPL36A-HNRNPH2)	NP_001186902.1:n.*622C=
NM_001199974.1:c.*622C= (RPL36A-HNRNPH2)	NP_001186903.1:n.*622C=
NM_019597.4:c.626C= (HNRNPH2)	NP_062543.1:p.Pro209=
NM_001199973.2:c.*622C= (RPL36A-HNRNPH2)	NP_001186902.2:n.*622C=
NM_001199974.2:c.*622C= (RPL36A-HNRNPH2)	NP_001186903.2:n.*622C=
NM_019597.5:c.626C= (HNRNPH2) MANE Select	NP_062543.1:p.Pro209=
NM_001032393.3:c.626C= (HNRNPH2)	NP_001027565.1:p.Pro209=