Linked Data
ClinVar Variation Id:
9435
dbSNP Id:
rs137852621
ExAC:
17:48245078 G / A
gnomAD v2:
17-48245078-G-A
gnomAD v3:
17-50167717-G-A
gnomAD v4:
17-50167717-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.50167717G>A , CM000679.2:g.50167717G>A | GRCh38 |
| NC_000017.10:g.48245078G>A , CM000679.1:g.48245078G>A | GRCh37 |
| NC_000017.9:g.45600077G>A | NCBI36 |
| NG_008889.1:g.6713G>A , LRG_203:g.6713G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000504073.2:c.293G>A | ENSP00000422030.2:p.Arg98His | |
| ENST00000511303.6:n.38-230G>A | ||
| ENST00000512526.2:c.293G>A | ENSP00000426606.2:p.Arg98His | |
| ENST00000682109.1:c.173G>A | ENSP00000508041.1:p.Arg58His | |
| ENST00000683226.1:n.3G>A | ||
| ENST00000683294.1:c.293G>A | ENSP00000508134.1:p.Arg98His | |
| ENST00000262018.8:c.293G>A MANE Select | ENSP00000262018.3:p.Arg98His | |
| ENST00000262018.7:c.293G>A | ENSP00000262018.3:p.Arg98His | |
| ENST00000344627.10:c.293G>A | ENSP00000345522.6:p.Arg98His | |
| ENST00000502555.5:c.158-230G>A | ENSP00000422817.1:n.158-230G>A | |
| ENST00000511303.5:c.34-230G>A | ENSP00000426104.1:n.34-230G>A | |
| ENST00000512526.1:c.137G>A | ||
| ENST00000513821.5:c.293G>A | ENSP00000426571.1:p.Arg98His | |
| ENST00000513942.5:n.104-230G>A | ||
| ENST00000514934.1:c.*19-230G>A | ENSP00000423168.1:n.*19-230G>A | |
| NM_000023.2:c.293G>A , LRG_203t1:c.293G>A | NP_000014.1:p.Arg98His | |
| NM_001135697.1:c.293G>A | NP_001129169.1:p.Arg98His | |
| XM_011525120.1:c.293G>A | XP_011523422.1:p.Arg98His | |
| XM_011525121.1:c.293G>A | XP_011523423.1:p.Arg98His | |
| XM_011525122.1:c.293G>A | XP_011523424.1:p.Arg98His | |
| XM_011525123.1:c.293G>A | XP_011523425.1:p.Arg98His | |
| XM_011525124.1:c.7-230G>A | XP_011523426.1:n.7-230G>A | |
| XR_934517.1:n.359G>A | ||
| NM_000023.3:c.293G>A | NP_000014.1:p.Arg98His | |
| NM_001135697.2:c.293G>A | NP_001129169.1:p.Arg98His | |
| NR_135553.1:n.349G>A | ||
| XM_011525120.2:c.455G>A | XP_011523422.2:p.Arg152His | |
| XM_011525121.2:c.455G>A | XP_011523423.2:p.Arg152His | |
| XM_011525122.2:c.455G>A | XP_011523424.2:p.Arg152His | |
| XM_011525123.2:c.455G>A | XP_011523425.2:p.Arg152His | |
| XM_011525124.2:c.7-230G>A | XP_011523426.1:n.7-230G>A | |
| XM_024450873.1:c.7-230G>A | XP_024306641.1:n.7-230G>A | |
| XR_002958056.1:n.811G>A | ||
| NM_000023.4:c.293G>A MANE Select | NP_000014.1:p.Arg98His | |
| NM_001135697.3:c.293G>A | NP_001129169.1:p.Arg98His | |
| NR_135553.2:n.329G>A |