Canonical Allele Identifier: CA413942880
Gene: HNRNPH2 HGNC NCBI
RPL36A-HNRNPH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101412737A>C , CM000685.2:g.101412737A>C GRCh38
NC_000023.10:g.100667725A>C , CM000685.1:g.100667725A>C GRCh37
NC_000023.9:g.100554381A>C NCBI36
NG_007119.1:g.227T>G , LRG_672:g.227T>G
NG_016327.1:g.9535A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000316594.6:c.749A>C (HNRNPH2) MANE Select ENSP00000361927.2:p.Asn250Thr
ENST00000316594.5:c.749A>C (HNRNPH2) ENSP00000361927.2:p.Asn250Thr
NM_001032393.2:c.749A>C (HNRNPH2) NP_001027565.1:p.Asn250Thr
NM_001199973.1:c.*745A>C (RPL36A-HNRNPH2) NP_001186902.1:n.*745A>C
NM_001199974.1:c.*745A>C (RPL36A-HNRNPH2) NP_001186903.1:n.*745A>C
NM_019597.4:c.749A>C (HNRNPH2) NP_062543.1:p.Asn250Thr
NM_001199973.2:c.*745A>C (RPL36A-HNRNPH2) NP_001186902.2:n.*745A>C
NM_001199974.2:c.*745A>C (RPL36A-HNRNPH2) NP_001186903.2:n.*745A>C
NM_019597.5:c.749A>C (HNRNPH2) MANE Select NP_062543.1:p.Asn250Thr
NM_001032393.3:c.749A>C (HNRNPH2) NP_001027565.1:p.Asn250Thr