Linked Data
ClinVar Variation Id:
205796
dbSNP Id:
rs150282556
ExAC:
17:44116561 G / A
gnomAD v2:
17-44116561-G-A
gnomAD v3:
17-46039195-G-A
gnomAD v4:
17-46039195-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.46039195G>A , CM000679.2:g.46039195G>A | GRCh38 |
| NC_000017.10:g.44116561G>A , CM000679.1:g.44116561G>A | GRCh37 |
| NC_000017.9:g.41472408G>A | NCBI36 |
| NG_032784.1:g.191180C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000432791.7:c.2224C>T MANE Select | ENSP00000387393.3:p.Arg742Trp | |
| ENST00000572904.6:c.2224C>T | ENSP00000461484.1:p.Arg742Trp | |
| ENST00000573286.2:n.3907C>T | ||
| ENST00000574590.6:c.2224C>T | ENSP00000461812.2:p.Arg742Trp | |
| ENST00000575318.6:c.2203+507C>T | ENSP00000461299.1:n.2203+507C>T | |
| ENST00000638275.1:c.2203+507C>T | ENSP00000492576.1:n.2203+507C>T | |
| ENST00000639150.1:c.958C>T | ENSP00000491906.1:p.Arg320Trp | |
| ENST00000639531.1:c.2203+507C>T | ENSP00000491765.1:n.2203+507C>T | |
| ENST00000639853.1:c.1374+507C>T | ||
| ENST00000640636.1:c.345+507C>T | ||
| ENST00000648792.1:c.2224C>T | ENSP00000497628.1:p.Arg742Trp | |
| ENST00000262419.10:c.2224C>T | ENSP00000262419.6:p.Arg742Trp | |
| ENST00000432791.5:c.2224C>T | ENSP00000387393.2:p.Arg742Trp | |
| ENST00000572218.5:n.6441C>T | ||
| ENST00000572679.1:n.356C>T | ||
| ENST00000572904.5:c.2224C>T | ENSP00000461484.1:p.Arg742Trp | |
| ENST00000573286.1:n.80C>T | ||
| ENST00000574590.5:c.2224C>T | ENSP00000461812.1:p.Arg742Trp | |
| ENST00000575318.5:c.2203+507C>T | ENSP00000461299.1:n.2203+507C>T | |
| ENST00000576870.5:n.364+507C>T | ||
| NM_001193465.1:c.2224C>T | NP_001180394.1:p.Arg742Trp | |
| NM_001193466.1:c.2224C>T | NP_001180395.1:p.Arg742Trp | |
| NM_015443.3:c.2224C>T | NP_056258.1:p.Arg742Trp | |
| XM_006721823.1:c.2224C>T | XP_006721886.1:p.Arg742Trp | |
| XM_006721824.2:c.2224C>T | XP_006721887.1:p.Arg742Trp | |
| XM_011524628.1:c.2224C>T | XP_011522930.1:p.Arg742Trp | |
| XM_011524629.1:c.2122C>T | XP_011522931.1:p.Arg708Trp | |
| XM_011524630.1:c.2203+507C>T | XP_011522932.1:n.2203+507C>T | |
| XM_011524631.1:c.2203+507C>T | XP_011522933.1:n.2203+507C>T | |
| XM_011524632.1:c.994C>T | XP_011522934.1:p.Arg332Trp | |
| XM_006721823.2:c.2224C>T | XP_006721886.1:p.Arg742Trp | |
| XM_006721824.4:c.2224C>T | XP_006721887.1:p.Arg742Trp | |
| XM_011524628.3:c.2224C>T | XP_011522930.1:p.Arg742Trp | |
| XM_011524629.3:c.2122C>T | XP_011522931.1:p.Arg708Trp | |
| XM_011524630.3:c.2203+507C>T | XP_011522932.1:n.2203+507C>T | |
| XM_011524631.3:c.2203+507C>T | XP_011522933.1:n.2203+507C>T | |
| XM_011524632.3:c.994C>T | XP_011522934.1:p.Arg332Trp | |
| XM_017024488.2:c.2203+507C>T | XP_016879977.1:n.2203+507C>T | |
| XM_017024489.1:c.2122C>T | XP_016879978.1:p.Arg708Trp | |
| NM_001193466.2:c.2224C>T | NP_001180395.1:p.Arg742Trp | |
| NM_015443.4:c.2224C>T MANE Select | NP_056258.1:p.Arg742Trp | |
| NM_001193465.2:c.2224C>T | NP_001180394.1:p.Arg742Trp | |
| NM_001379198.1:c.2224C>T | NP_001366127.1:p.Arg742Trp |