Canonical Allele Identifier: CA2448303073
Gene: HNRNPH2 HGNC NCBI
RPL36A-HNRNPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101412706T= , CM000685.2:g.101412706T= GRCh38
NC_000023.10:g.100667694T= , CM000685.1:g.100667694T= GRCh37
NC_000023.9:g.100554350T= NCBI36
NG_007119.1:g.258A= , LRG_672:g.258A=
NG_016327.1:g.9504T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000316594.6:c.718T= (HNRNPH2) MANE Select ENSP00000361927.2:p.Tyr240=
ENST00000316594.5:c.718T= (HNRNPH2) ENSP00000361927.2:p.Tyr240=
NM_001032393.2:c.718T= (HNRNPH2) NP_001027565.1:p.Tyr240=
NM_001199973.1:c.*714T= (RPL36A-HNRNPH2) NP_001186902.1:n.*714T=
NM_001199974.1:c.*714T= (RPL36A-HNRNPH2) NP_001186903.1:n.*714T=
NM_019597.4:c.718T= (HNRNPH2) NP_062543.1:p.Tyr240=
NM_001199973.2:c.*714T= (RPL36A-HNRNPH2) NP_001186902.2:n.*714T=
NM_001199974.2:c.*714T= (RPL36A-HNRNPH2) NP_001186903.2:n.*714T=
NM_019597.5:c.718T= (HNRNPH2) MANE Select NP_062543.1:p.Tyr240=
NM_001032393.3:c.718T= (HNRNPH2) NP_001027565.1:p.Tyr240=