Canonical Allele Identifier: CA2448303079
Gene: HNRNPH2 HGNC NCBI
RPL36A-HNRNPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101412732C= , CM000685.2:g.101412732C= GRCh38
NC_000023.10:g.100667720C= , CM000685.1:g.100667720C= GRCh37
NC_000023.9:g.100554376C= NCBI36
NG_007119.1:g.232G= , LRG_672:g.232G=
NG_016327.1:g.9530C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000316594.6:c.744C= (HNRNPH2) MANE Select ENSP00000361927.2:p.Gly248=
ENST00000316594.5:c.744C= (HNRNPH2) ENSP00000361927.2:p.Gly248=
NM_001032393.2:c.744C= (HNRNPH2) NP_001027565.1:p.Gly248=
NM_001199973.1:c.*740C= (RPL36A-HNRNPH2) NP_001186902.1:n.*740C=
NM_001199974.1:c.*740C= (RPL36A-HNRNPH2) NP_001186903.1:n.*740C=
NM_019597.4:c.744C= (HNRNPH2) NP_062543.1:p.Gly248=
NM_001199973.2:c.*740C= (RPL36A-HNRNPH2) NP_001186902.2:n.*740C=
NM_001199974.2:c.*740C= (RPL36A-HNRNPH2) NP_001186903.2:n.*740C=
NM_019597.5:c.744C= (HNRNPH2) MANE Select NP_062543.1:p.Gly248=
NM_001032393.3:c.744C= (HNRNPH2) NP_001027565.1:p.Gly248=