Linked Data
ClinVar Variation Id:
461412
dbSNP Id:
rs570139975
ExAC:
20:62038529 G / A
gnomAD v2:
20-62038529-G-A
gnomAD v3:
20-63407176-G-A
gnomAD v4:
20-63407176-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.63407176G>A , CM000682.2:g.63407176G>A | GRCh38 |
| NC_000020.10:g.62038529G>A , CM000682.1:g.62038529G>A | GRCh37 |
| NC_000020.9:g.61508973G>A | NCBI36 |
| NG_009004.1:g.70465C>T | |
| NG_009004.2:g.70465C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000706989.1:c.2141C>T | ENSP00000516702.1:p.Thr714Met | |
| ENST00000359125.7:c.2087C>T MANE Select | ENSP00000352035.2:p.Thr696Met | |
| ENST00000637193.1:c.1484C>T | ENSP00000490734.1:p.Thr495Met | |
| ENST00000344462.8:c.1994C>T | ENSP00000339611.4:p.Thr665Met | |
| ENST00000357249.6:c.1655C>T | ENSP00000349789.3:p.Thr552Met | |
| ENST00000359125.6:c.2087C>T | ENSP00000352035.2:p.Thr696Met | |
| ENST00000360480.7:c.2003C>T | ENSP00000353668.3:p.Thr668Met | |
| ENST00000370224.5:c.2111C>T | ENSP00000359244.2:p.Thr704Met | |
| ENST00000625514.2:c.2075C>T | ENSP00000486040.1:p.Thr692Met | |
| ENST00000626839.2:c.2033C>T | ENSP00000486706.1:p.Thr678Met | |
| ENST00000629241.2:c.2003C>T | ENSP00000487142.1:p.Thr668Met | |
| ENST00000629676.2:c.1679+6274C>T | ENSP00000486194.1:n.1679+6274C>T | |
| NM_004518.4:c.2003C>T | NP_004509.2:p.Thr668Met | |
| NM_172106.1:c.2033C>T | NP_742104.1:p.Thr678Met | |
| NM_172107.2:c.2087C>T | NP_742105.1:p.Thr696Met | |
| NM_172108.3:c.1994C>T | NP_742106.1:p.Thr665Met | |
| XM_006723787.1:c.2129C>T | XP_006723850.1:p.Thr710Met | |
| XM_011528807.1:c.2195C>T | XP_011527109.1:p.Thr732Met | |
| XM_011528808.1:c.2192C>T | XP_011527110.1:p.Thr731Met | |
| XM_011528809.1:c.2165C>T | XP_011527111.1:p.Thr722Met | |
| XM_011528810.1:c.2141C>T | XP_011527112.1:p.Thr714Met | |
| XM_011528811.1:c.2111C>T | XP_011527113.1:p.Thr704Met | |
| XM_011528812.1:c.2084C>T | XP_011527114.1:p.Thr695Met | |
| XM_011528813.1:c.2069C>T | XP_011527115.1:p.Thr690Met | |
| XM_011528814.1:c.1676C>T | XP_011527116.1:p.Thr559Met | |
| NM_004518.5:c.2003C>T | NP_004509.2:p.Thr668Met | |
| NM_172106.2:c.2033C>T | NP_742104.1:p.Thr678Met | |
| NM_172107.3:c.2087C>T | NP_742105.1:p.Thr696Met | |
| NM_172108.4:c.1994C>T | NP_742106.1:p.Thr665Met | |
| XM_011528810.2:c.2141C>T | XP_011527112.1:p.Thr714Met | |
| XM_011528811.2:c.2111C>T | XP_011527113.1:p.Thr704Met | |
| XM_017027841.2:c.2138C>T | XP_016883330.1:p.Thr713Met | |
| XM_017027842.2:c.2075C>T | XP_016883331.1:p.Thr692Met | |
| XM_017027843.1:c.2072C>T | XP_016883332.1:p.Thr691Met | |
| XM_017027844.2:c.2030C>T | XP_016883333.1:p.Thr677Met | |
| XM_017027845.1:c.1103C>T | XP_016883334.1:p.Thr368Met | |
| NM_004518.6:c.2003C>T | NP_004509.2:p.Thr668Met | |
| NM_172106.3:c.2033C>T | NP_742104.1:p.Thr678Met | |
| NM_172107.4:c.2087C>T MANE Select | NP_742105.1:p.Thr696Met | |
| NM_172108.5:c.1994C>T | NP_742106.1:p.Thr665Met | |
| NM_001382235.1:c.2141C>T | NP_001369164.1:p.Thr714Met |