Linked Data
dbSNP Id:
rs782374129
ExAC:
X:100667425 G / A
gnomAD v2:
X-100667425-G-A
gnomAD v4:
X-101412437-G-A
COSMIC:
COSM1682772
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.101412437G>A , CM000685.2:g.101412437G>A | GRCh38 |
| NC_000023.10:g.100667425G>A , CM000685.1:g.100667425G>A | GRCh37 |
| NC_000023.9:g.100554081G>A | NCBI36 |
| NG_007119.1:g.527C>T , LRG_672:g.527C>T | |
| NG_016327.1:g.9235G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000316594.6:c.449G>A (HNRNPH2) MANE Select | ENSP00000361927.2:p.Arg150Gln | |
| ENST00000316594.5:c.449G>A (HNRNPH2) | ENSP00000361927.2:p.Arg150Gln | |
| NM_001032393.2:c.449G>A (HNRNPH2) | NP_001027565.1:p.Arg150Gln | |
| NM_001199973.1:c.*445G>A (RPL36A-HNRNPH2) | NP_001186902.1:n.*445G>A | |
| NM_001199974.1:c.*445G>A (RPL36A-HNRNPH2) | NP_001186903.1:n.*445G>A | |
| NM_019597.4:c.449G>A (HNRNPH2) | NP_062543.1:p.Arg150Gln | |
| NM_001199973.2:c.*445G>A (RPL36A-HNRNPH2) | NP_001186902.2:n.*445G>A | |
| NM_001199974.2:c.*445G>A (RPL36A-HNRNPH2) | NP_001186903.2:n.*445G>A | |
| NM_019597.5:c.449G>A (HNRNPH2) MANE Select | NP_062543.1:p.Arg150Gln | |
| NM_001032393.3:c.449G>A (HNRNPH2) | NP_001027565.1:p.Arg150Gln |