Canonical Allele Identifier: CA413942261
Gene: HNRNPH2 HGNC NCBI
RPL36A-HNRNPH2 HGNC NCBI

Linked Data

gnomAD v4: X-101412467-C-T
MyVariant Identifiers: chrX:g.100667455C>T (hg19) chrX:g.101412467C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101412467C>T , CM000685.2:g.101412467C>T GRCh38
NC_000023.10:g.100667455C>T , CM000685.1:g.100667455C>T GRCh37
NC_000023.9:g.100554111C>T NCBI36
NG_007119.1:g.497G>A , LRG_672:g.497G>A
NG_016327.1:g.9265C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000316594.6:c.479C>T (HNRNPH2) MANE Select ENSP00000361927.2:p.Ala160Val
ENST00000316594.5:c.479C>T (HNRNPH2) ENSP00000361927.2:p.Ala160Val
NM_001032393.2:c.479C>T (HNRNPH2) NP_001027565.1:p.Ala160Val
NM_001199973.1:c.*475C>T (RPL36A-HNRNPH2) NP_001186902.1:n.*475C>T
NM_001199974.1:c.*475C>T (RPL36A-HNRNPH2) NP_001186903.1:n.*475C>T
NM_019597.4:c.479C>T (HNRNPH2) NP_062543.1:p.Ala160Val
NM_001199973.2:c.*475C>T (RPL36A-HNRNPH2) NP_001186902.2:n.*475C>T
NM_001199974.2:c.*475C>T (RPL36A-HNRNPH2) NP_001186903.2:n.*475C>T
NM_019597.5:c.479C>T (HNRNPH2) MANE Select NP_062543.1:p.Ala160Val
NM_001032393.3:c.479C>T (HNRNPH2) NP_001027565.1:p.Ala160Val
Search 100 bp 5'
Search 100 bp 3'