Linked Data
dbSNP Id:
rs774157742
ExAC:
11:68701324 G / A
gnomAD v2:
11-68701324-G-A
gnomAD v3:
11-68933856-G-A
gnomAD v4:
11-68933856-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.68933856G>A , CM000673.2:g.68933856G>A | GRCh38 |
| NC_000011.9:g.68701324G>A , CM000673.1:g.68701324G>A | GRCh37 |
| NC_000011.8:g.68457900G>A | NCBI36 |
| NG_007976.1:g.35006G>A , LRG_250:g.35006G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000255078.8:c.1480G>A MANE Select | ENSP00000255078.4:p.Ala494Thr | |
| ENST00000674955.1:c.*197G>A | ENSP00000502463.1:n.*197G>A | |
| ENST00000675118.1:c.968G>A | ||
| ENST00000675205.1:n.183+375G>A | ||
| ENST00000675615.1:c.1480G>A | ENSP00000502413.1:p.Ala494Thr | |
| ENST00000675648.1:n.855G>A | ||
| ENST00000675997.1:n.113-608G>A | ||
| ENST00000676173.1:n.2225G>A | ||
| ENST00000676228.1:c.*803G>A | ENSP00000502375.1:n.*803G>A | |
| ENST00000255078.7:c.1480G>A | ENSP00000255078.3:p.Ala494Thr | |
| ENST00000537458.5:n.597G>A | ||
| ENST00000539064.5:n.1239G>A | ||
| ENST00000541229.5:n.175G>A | ||
| ENST00000543739.5:n.597G>A | ||
| NM_002180.2:c.1480G>A , LRG_250t1:c.1480G>A | NP_002171.2:p.Ala494Thr | |
| XM_005273974.2:c.469G>A | XP_005274031.1:p.Ala157Thr | |
| XM_005273975.2:c.352G>A | XP_005274032.1:p.Ala118Thr | |
| XM_011544994.1:c.247G>A | XP_011543296.1:p.Ala83Thr | |
| XR_949903.1:n.1582G>A | ||
| XM_005273975.3:c.352G>A | XP_005274032.1:p.Ala118Thr | |
| XM_017017669.2:c.469G>A | XP_016873158.1:p.Ala157Thr | |
| XM_017017670.2:c.469G>A | XP_016873159.1:p.Ala157Thr | |
| XM_017017671.2:c.1480G>A | XP_016873160.1:p.Ala494Thr | |
| XR_949903.3:n.1578G>A | ||
| NM_002180.3:c.1480G>A MANE Select | NP_002171.2:p.Ala494Thr |