Canonical Allele Identifier: CA413942323

Gene: HNRNPH2 RPL36A-HNRNPH2

Linked Data

• MyVariant Identifiers: chrX:g.100667482T>G (hg19) ; chrX:g.101412494T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101412494T>G , CM000685.2:g.101412494T>G	GRCh38
NC_000023.10:g.100667482T>G , CM000685.1:g.100667482T>G	GRCh37
NC_000023.9:g.100554138T>G	NCBI36
NG_007119.1:g.470A>C , LRG_672:g.470A>C
NG_016327.1:g.9292T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316594.6:c.506T>G (HNRNPH2) MANE Select	ENSP00000361927.2:p.Leu169Ter
ENST00000316594.5:c.506T>G (HNRNPH2)	ENSP00000361927.2:p.Leu169Ter
NM_001032393.2:c.506T>G (HNRNPH2)	NP_001027565.1:p.Leu169Ter
NM_001199973.1:c.*502T>G (RPL36A-HNRNPH2)	NP_001186902.1:n.*502T>G
NM_001199974.1:c.*502T>G (RPL36A-HNRNPH2)	NP_001186903.1:n.*502T>G
NM_019597.4:c.506T>G (HNRNPH2)	NP_062543.1:p.Leu169Ter
NM_001199973.2:c.*502T>G (RPL36A-HNRNPH2)	NP_001186902.2:n.*502T>G
NM_001199974.2:c.*502T>G (RPL36A-HNRNPH2)	NP_001186903.2:n.*502T>G
NM_019597.5:c.506T>G (HNRNPH2) MANE Select	NP_062543.1:p.Leu169Ter
NM_001032393.3:c.506T>G (HNRNPH2)	NP_001027565.1:p.Leu169Ter