Canonical Allele Identifier: CA413943491
Gene: HNRNPH2 HGNC NCBI
RPL36A-HNRNPH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101412869G>C , CM000685.2:g.101412869G>C GRCh38
NC_000023.10:g.100667857G>C , CM000685.1:g.100667857G>C GRCh37
NC_000023.9:g.100554513G>C NCBI36
NG_007119.1:g.95C>G , LRG_672:g.95C>G
NG_016327.1:g.9667G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000316594.6:c.881G>C (HNRNPH2) MANE Select ENSP00000361927.2:p.Arg294Thr
ENST00000316594.5:c.881G>C (HNRNPH2) ENSP00000361927.2:p.Arg294Thr
NM_001032393.2:c.881G>C (HNRNPH2) NP_001027565.1:p.Arg294Thr
NM_001199973.1:c.*877G>C (RPL36A-HNRNPH2) NP_001186902.1:n.*877G>C
NM_001199974.1:c.*877G>C (RPL36A-HNRNPH2) NP_001186903.1:n.*877G>C
NM_019597.4:c.881G>C (HNRNPH2) NP_062543.1:p.Arg294Thr
NM_001199973.2:c.*877G>C (RPL36A-HNRNPH2) NP_001186902.2:n.*877G>C
NM_001199974.2:c.*877G>C (RPL36A-HNRNPH2) NP_001186903.2:n.*877G>C
NM_019597.5:c.881G>C (HNRNPH2) MANE Select NP_062543.1:p.Arg294Thr
NM_001032393.3:c.881G>C (HNRNPH2) NP_001027565.1:p.Arg294Thr