Linked Data
ClinVar Variation Id:
2976331
ClinVar RCV Id:
RCV003836481
dbSNP Id:
rs752648281
gnomAD v2:
18-43490530-G-A
gnomAD v4:
18-45910565-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.45910565G>A , CM000680.2:g.45910565G>A | GRCh38 |
| NC_000018.9:g.43490530G>A , CM000680.1:g.43490530G>A | GRCh37 |
| NC_000018.8:g.41744528G>A | NCBI36 |
| NG_042838.1:g.61775C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000586655.2:n.2345C>T | ||
| ENST00000587884.2:c.4161C>T | ENSP00000466990.2:p.Thr1387= | |
| ENST00000590884.6:c.4161C>T | ENSP00000466403.2:p.Thr1387= | |
| ENST00000592272.6:c.4161C>T | ENSP00000467464.2:p.Thr1387= | |
| ENST00000696482.1:c.3901C>T | ENSP00000512656.1:n.3901C>T | |
| ENST00000696483.1:c.4161C>T | ENSP00000512657.1:p.Thr1387= | |
| ENST00000696484.1:c.4161C>T | ENSP00000512658.1:p.Thr1387= | |
| ENST00000696485.1:c.4161C>T | ENSP00000512659.1:p.Thr1387= | |
| ENST00000696489.1:c.4161C>T | ENSP00000512660.1:p.Thr1387= | |
| ENST00000696490.1:c.4161C>T | ENSP00000512661.1:p.Thr1387= | |
| ENST00000282041.11:c.4161C>T MANE Select | ENSP00000282041.4:p.Thr1387= | |
| ENST00000282041.9:c.4161C>T | ENSP00000282041.4:p.Thr1387= | |
| ENST00000585906.5:n.940C>T | ||
| ENST00000587884.1:c.786C>T | ENSP00000466990.1:p.Thr262= | |
| ENST00000587974.1:n.4196C>T | ||
| ENST00000590884.5:c.786C>T | ENSP00000466403.1:p.Thr262= | |
| ENST00000592272.5:c.786C>T | ENSP00000467464.1:p.Thr262= | |
| NM_020964.2:c.4161C>T | NP_066015.2:p.Thr1387= | |
| XM_011526120.1:c.4188C>T | XP_011524422.1:p.Thr1396= | |
| XM_011526121.1:c.4188C>T | XP_011524423.1:p.Thr1396= | |
| XM_011526122.1:c.4161C>T | XP_011524424.1:p.Thr1387= | |
| XM_011526123.1:c.4188C>T | XP_011524425.1:p.Thr1396= | |
| XM_011526124.1:c.4188C>T | XP_011524426.1:p.Thr1396= | |
| XM_011526125.1:c.4047C>T | XP_011524427.1:p.Thr1349= | |
| XM_011526126.1:c.3123C>T | XP_011524428.1:p.Thr1041= | |
| XM_011526127.1:c.4188C>T | XP_011524429.1:p.Thr1396= | |
| XM_011526128.1:c.4188C>T | XP_011524430.1:p.Thr1396= | |
| XR_935244.1:n.4261C>T | ||
| NM_020964.3:c.4161C>T MANE Select | NP_066015.2:p.Thr1387= | |
| XM_017025889.1:c.4161C>T | XP_016881378.1:p.Thr1387= | |
| XM_017025890.2:c.4161C>T | XP_016881379.1:p.Thr1387= | |
| XM_017025891.1:c.4020C>T | XP_016881380.1:p.Thr1340= | |
| XM_017025892.1:c.3096C>T | XP_016881381.1:p.Thr1032= | |
| XM_017025893.1:c.786C>T | XP_016881382.1:p.Thr262= | |
| XR_001753256.1:n.4243C>T | ||
| XR_001753257.1:n.4243C>T |