Canonical Allele Identifier: CA413943442
Gene: HNRNPH2 HGNC NCBI
RPL36A-HNRNPH2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.100667848T>G (hg19) chrX:g.101412860T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101412860T>G , CM000685.2:g.101412860T>G GRCh38
NC_000023.10:g.100667848T>G , CM000685.1:g.100667848T>G GRCh37
NC_000023.9:g.100554504T>G NCBI36
NG_007119.1:g.104A>C , LRG_672:g.104A>C
NG_016327.1:g.9658T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000316594.6:c.872T>G (HNRNPH2) MANE Select ENSP00000361927.2:p.Val291Gly
ENST00000316594.5:c.872T>G (HNRNPH2) ENSP00000361927.2:p.Val291Gly
NM_001032393.2:c.872T>G (HNRNPH2) NP_001027565.1:p.Val291Gly
NM_001199973.1:c.*868T>G (RPL36A-HNRNPH2) NP_001186902.1:n.*868T>G
NM_001199974.1:c.*868T>G (RPL36A-HNRNPH2) NP_001186903.1:n.*868T>G
NM_019597.4:c.872T>G (HNRNPH2) NP_062543.1:p.Val291Gly
NM_001199973.2:c.*868T>G (RPL36A-HNRNPH2) NP_001186902.2:n.*868T>G
NM_001199974.2:c.*868T>G (RPL36A-HNRNPH2) NP_001186903.2:n.*868T>G
NM_019597.5:c.872T>G (HNRNPH2) MANE Select NP_062543.1:p.Val291Gly
NM_001032393.3:c.872T>G (HNRNPH2) NP_001027565.1:p.Val291Gly
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