Canonical Allele Identifier: CA2448303007
Gene: HNRNPH2 HGNC NCBI
RPL36A-HNRNPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101412325G= , CM000685.2:g.101412325G= GRCh38
NC_000023.10:g.100667313G= , CM000685.1:g.100667313G= GRCh37
NC_000023.9:g.100553969G= NCBI36
NG_007119.1:g.639C= , LRG_672:g.639C=
NG_016327.1:g.9123G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000316594.6:c.337G= (HNRNPH2) MANE Select ENSP00000361927.2:p.Val113=
ENST00000316594.5:c.337G= (HNRNPH2) ENSP00000361927.2:p.Val113=
NM_001032393.2:c.337G= (HNRNPH2) NP_001027565.1:p.Val113=
NM_001199973.1:c.*333G= (RPL36A-HNRNPH2) NP_001186902.1:n.*333G=
NM_001199974.1:c.*333G= (RPL36A-HNRNPH2) NP_001186903.1:n.*333G=
NM_019597.4:c.337G= (HNRNPH2) NP_062543.1:p.Val113=
NM_001199973.2:c.*333G= (RPL36A-HNRNPH2) NP_001186902.2:n.*333G=
NM_001199974.2:c.*333G= (RPL36A-HNRNPH2) NP_001186903.2:n.*333G=
NM_019597.5:c.337G= (HNRNPH2) MANE Select NP_062543.1:p.Val113=
NM_001032393.3:c.337G= (HNRNPH2) NP_001027565.1:p.Val113=