Linked Data
dbSNP Id:
rs2149735995
gnomAD v4:
5-177093546-G-A
MyVariant Identifiers:
chr5:g.176520547G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.177093546G>A , CM000667.2:g.177093546G>A | GRCh38 |
| NC_000005.9:g.176520547G>A , CM000667.1:g.176520547G>A | GRCh37 |
| NC_000005.8:g.176453153G>A | NCBI36 |
| NG_012067.1:g.11627G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000292408.9:c.1392G>A MANE Select | ENSP00000292408.4:p.Arg464= | |
| ENST00000292408.8:c.1392G>A | ENSP00000292408.4:p.Arg464= | |
| ENST00000393637.5:c.1272G>A | ENSP00000377254.1:p.Arg424= | |
| ENST00000393648.6:c.1193+45G>A | ENSP00000377259.2:n.1193+45G>A | |
| ENST00000502906.5:c.1392G>A | ENSP00000424960.1:p.Arg464= | |
| ENST00000511076.1:c.286G>A | ||
| NM_001291980.1:c.1193+45G>A | NP_001278909.1:n.1193+45G>A | |
| NM_002011.4:c.1392G>A | NP_002002.3:p.Arg464= | |
| NM_022963.3:c.1272G>A | NP_075252.2:p.Arg424= | |
| NM_213647.2:c.1392G>A | NP_998812.1:p.Arg464= | |
| XM_005265838.2:c.1392G>A | XP_005265895.1:p.Arg464= | |
| XM_011534464.1:c.1485G>A | XP_011532766.1:p.Arg495= | |
| XM_011534465.1:c.1074G>A | XP_011532767.1:p.Arg358= | |
| XR_941090.1:n.1392+45G>A | ||
| NM_001354984.1:c.1392G>A | NP_001341913.1:p.Arg464= | |
| NM_213647.3:c.1392G>A MANE Select | NP_998812.1:p.Arg464= | |
| NM_001291980.2:c.1193+45G>A | NP_001278909.1:n.1193+45G>A | |
| NM_001354984.2:c.1392G>A | NP_001341913.1:p.Arg464= | |
| NM_002011.5:c.1392G>A | NP_002002.3:p.Arg464= |