Linked Data
ClinVar Variation Id:
2055420
ClinVar RCV Id:
RCV002947243
dbSNP Id:
rs750809033
ExAC:
2:25965019 G / A
gnomAD v2:
2-25965019-G-A
gnomAD v3:
2-25742150-G-A
gnomAD v4:
2-25742150-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.25742150G>A , CM000664.2:g.25742150G>A | GRCh38 |
| NC_000002.11:g.25965019G>A , CM000664.1:g.25965019G>A | GRCh37 |
| NC_000002.10:g.25818523G>A | NCBI36 |
| NG_052995.1:g.141367C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000336112.9:c.4184C>T | ENSP00000337250.5:p.Thr1395Met | |
| ENST00000435504.9:c.4187C>T MANE Select | ENSP00000391447.3:p.Thr1396Met | |
| ENST00000336112.8:c.4103C>T | ENSP00000337250.4:p.Thr1368Met | |
| ENST00000404843.5:c.2636C>T | ENSP00000383920.1:p.Thr879Met | |
| ENST00000435504.8:c.4187C>T | ENSP00000391447.3:p.Thr1396Met | |
| NM_018263.4:c.4187C>T | NP_060733.4:p.Thr1396Met | |
| XM_006712039.2:c.3821C>T | XP_006712102.1:p.Thr1274Met | |
| XM_006712040.1:c.3407C>T | XP_006712103.1:p.Thr1136Met | |
| XM_011532950.1:c.4184C>T | XP_011531252.1:p.Thr1395Met | |
| XM_011532951.1:c.4013C>T | XP_011531253.1:p.Thr1338Met | |
| NM_018263.5:c.4187C>T | NP_060733.4:p.Thr1396Met | |
| XM_006712039.3:c.3821C>T | XP_006712102.1:p.Thr1274Met | |
| XM_006712040.2:c.3407C>T | XP_006712103.1:p.Thr1136Met | |
| XM_011532950.3:c.4184C>T | XP_011531252.1:p.Thr1395Met | |
| XM_011532951.2:c.4013C>T | XP_011531253.1:p.Thr1338Met | |
| XM_017004430.1:c.3407C>T | XP_016859919.1:p.Thr1136Met | |
| XM_024452974.1:c.4367C>T | XP_024308742.1:p.Thr1456Met | |
| NM_001369346.1:c.4013C>T | NP_001356275.1:p.Thr1338Met | |
| NM_001369347.1:c.3407C>T | NP_001356276.1:p.Thr1136Met | |
| NM_018263.6:c.4187C>T MANE Select | NP_060733.4:p.Thr1396Met |