Canonical Allele Identifier: CA2448303013
Gene: HNRNPH2 HGNC NCBI
RPL36A-HNRNPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101412369T= , CM000685.2:g.101412369T= GRCh38
NC_000023.10:g.100667357T= , CM000685.1:g.100667357T= GRCh37
NC_000023.9:g.100554013T= NCBI36
NG_007119.1:g.595A= , LRG_672:g.595A=
NG_016327.1:g.9167T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000316594.6:c.381T= (HNRNPH2) MANE Select ENSP00000361927.2:p.Ile127=
ENST00000316594.5:c.381T= (HNRNPH2) ENSP00000361927.2:p.Ile127=
NM_001032393.2:c.381T= (HNRNPH2) NP_001027565.1:p.Ile127=
NM_001199973.1:c.*377T= (RPL36A-HNRNPH2) NP_001186902.1:n.*377T=
NM_001199974.1:c.*377T= (RPL36A-HNRNPH2) NP_001186903.1:n.*377T=
NM_019597.4:c.381T= (HNRNPH2) NP_062543.1:p.Ile127=
NM_001199973.2:c.*377T= (RPL36A-HNRNPH2) NP_001186902.2:n.*377T=
NM_001199974.2:c.*377T= (RPL36A-HNRNPH2) NP_001186903.2:n.*377T=
NM_019597.5:c.381T= (HNRNPH2) MANE Select NP_062543.1:p.Ile127=
NM_001032393.3:c.381T= (HNRNPH2) NP_001027565.1:p.Ile127=