Canonical Allele Identifier: CA517737553
Gene: HNRNPH2 HGNC NCBI
RPL36A-HNRNPH2 HGNC NCBI

Linked Data

gnomAD v4: X-101412846-C-A
MyVariant Identifiers: chrX:g.100667834C>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101412846C>A , CM000685.2:g.101412846C>A GRCh38
NC_000023.10:g.100667834C>A , CM000685.1:g.100667834C>A GRCh37
NC_000023.9:g.100554490C>A NCBI36
NG_007119.1:g.118G>T , LRG_672:g.118G>T
NG_016327.1:g.9644C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000316594.6:c.858C>A (HNRNPH2) MANE Select ENSP00000361927.2:p.Thr286=
ENST00000316594.5:c.858C>A (HNRNPH2) ENSP00000361927.2:p.Thr286=
NM_001032393.2:c.858C>A (HNRNPH2) NP_001027565.1:p.Thr286=
NM_001199973.1:c.*854C>A (RPL36A-HNRNPH2) NP_001186902.1:n.*854C>A
NM_001199974.1:c.*854C>A (RPL36A-HNRNPH2) NP_001186903.1:n.*854C>A
NM_019597.4:c.858C>A (HNRNPH2) NP_062543.1:p.Thr286=
NM_001199973.2:c.*854C>A (RPL36A-HNRNPH2) NP_001186902.2:n.*854C>A
NM_001199974.2:c.*854C>A (RPL36A-HNRNPH2) NP_001186903.2:n.*854C>A
NM_019597.5:c.858C>A (HNRNPH2) MANE Select NP_062543.1:p.Thr286=
NM_001032393.3:c.858C>A (HNRNPH2) NP_001027565.1:p.Thr286=
Search 100 bp 5'
Search 100 bp 3'