Canonical Allele Identifier: CA413942738
Gene: HNRNPH2 HGNC NCBI
RPL36A-HNRNPH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101412675A>T , CM000685.2:g.101412675A>T GRCh38
NC_000023.10:g.100667663A>T , CM000685.1:g.100667663A>T GRCh37
NC_000023.9:g.100554319A>T NCBI36
NG_007119.1:g.289T>A , LRG_672:g.289T>A
NG_016327.1:g.9473A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000316594.6:c.687A>T (HNRNPH2) MANE Select ENSP00000361927.2:p.Glu229Asp
ENST00000316594.5:c.687A>T (HNRNPH2) ENSP00000361927.2:p.Glu229Asp
NM_001032393.2:c.687A>T (HNRNPH2) NP_001027565.1:p.Glu229Asp
NM_001199973.1:c.*683A>T (RPL36A-HNRNPH2) NP_001186902.1:n.*683A>T
NM_001199974.1:c.*683A>T (RPL36A-HNRNPH2) NP_001186903.1:n.*683A>T
NM_019597.4:c.687A>T (HNRNPH2) NP_062543.1:p.Glu229Asp
NM_001199973.2:c.*683A>T (RPL36A-HNRNPH2) NP_001186902.2:n.*683A>T
NM_001199974.2:c.*683A>T (RPL36A-HNRNPH2) NP_001186903.2:n.*683A>T
NM_019597.5:c.687A>T (HNRNPH2) MANE Select NP_062543.1:p.Glu229Asp
NM_001032393.3:c.687A>T (HNRNPH2) NP_001027565.1:p.Glu229Asp