Canonical Allele Identifier: CA2448303024
Gene: HNRNPH2 HGNC NCBI
RPL36A-HNRNPH2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101412462G= , CM000685.2:g.101412462G= GRCh38
NC_000023.10:g.100667450G= , CM000685.1:g.100667450G= GRCh37
NC_000023.9:g.100554106G= NCBI36
NG_007119.1:g.502C= , LRG_672:g.502C=
NG_016327.1:g.9260G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000316594.6:c.474G= (HNRNPH2) MANE Select ENSP00000361927.2:p.Gln158=
ENST00000316594.5:c.474G= (HNRNPH2) ENSP00000361927.2:p.Gln158=
NM_001032393.2:c.474G= (HNRNPH2) NP_001027565.1:p.Gln158=
NM_001199973.1:c.*470G= (RPL36A-HNRNPH2) NP_001186902.1:n.*470G=
NM_001199974.1:c.*470G= (RPL36A-HNRNPH2) NP_001186903.1:n.*470G=
NM_019597.4:c.474G= (HNRNPH2) NP_062543.1:p.Gln158=
NM_001199973.2:c.*470G= (RPL36A-HNRNPH2) NP_001186902.2:n.*470G=
NM_001199974.2:c.*470G= (RPL36A-HNRNPH2) NP_001186903.2:n.*470G=
NM_019597.5:c.474G= (HNRNPH2) MANE Select NP_062543.1:p.Gln158=
NM_001032393.3:c.474G= (HNRNPH2) NP_001027565.1:p.Gln158=
Search 100 bp 5'
Search 100 bp 3'