Linked Data
dbSNP Id:
rs2087540282
gnomAD v4:
20-3671620-C-A
MyVariant Identifiers:
chr20:g.3652267C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.3671620C>A , CM000682.2:g.3671620C>A | GRCh38 |
| NC_000020.10:g.3652267C>A , CM000682.1:g.3652267C>A | GRCh37 |
| NC_000020.9:g.3600267C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000356518.7:c.1866G>T MANE Select | ENSP00000348912.3:p.Leu622= | |
| ENST00000350009.6:c.1866G>T | ENSP00000322550.5:p.Leu622= | |
| ENST00000356518.6:c.1866G>T | ENSP00000348912.2:p.Leu622= | |
| ENST00000379861.8:c.1866G>T | ENSP00000369190.4:p.Leu622= | |
| ENST00000466620.5:n.1505G>T | ||
| ENST00000617732.1:c.*632-163G>T | ENSP00000483343.1:n.*632-163G>T | |
| ENST00000619289.4:c.1506G>T | ENSP00000484600.1:p.Leu502= | |
| NM_001282447.1:c.1866G>T | NP_001269376.1:p.Leu622= | |
| NM_025220.3:c.1866G>T | NP_079496.1:p.Leu622= | |
| NM_153202.2:c.1866G>T | NP_694882.1:p.Leu622= | |
| XM_005260843.1:c.1905G>T | XP_005260900.1:p.Leu635= | |
| XM_006723639.1:c.1905G>T | XP_006723702.1:p.Leu635= | |
| XM_006723640.1:c.1896G>T | XP_006723703.1:p.Leu632= | |
| XM_011529366.1:c.1902G>T | XP_011527668.1:p.Leu634= | |
| XM_011529367.1:c.1863G>T | XP_011527669.1:p.Leu621= | |
| XM_011529368.1:c.1905G>T | XP_011527670.1:p.Leu635= | |
| XM_011529369.1:c.1873G>T | XP_011527671.1:p.Gly625Trp | |
| XM_011529370.1:c.1873G>T | XP_011527672.1:p.Gly625Trp | |
| XM_011529373.1:c.903G>T | XP_011527675.1:p.Leu301= | |
| XR_937151.1:n.2009G>T | ||
| XR_937152.1:n.2009G>T | ||
| XR_937153.1:n.1890G>T | ||
| XR_937154.1:n.1890G>T | ||
| XR_937155.1:n.1811G>T | ||
| XR_937157.1:n.1813G>T | ||
| NM_001282447.2:c.1866G>T | NP_001269376.1:p.Leu622= | |
| NM_025220.4:c.1866G>T | NP_079496.1:p.Leu622= | |
| NM_153202.3:c.1866G>T | NP_694882.1:p.Leu622= | |
| XM_011529373.2:c.903G>T | XP_011527675.1:p.Leu301= | |
| XR_001754405.1:n.1977G>T | ||
| XR_002958534.1:n.2086G>T | ||
| NM_001282447.3:c.1866G>T | NP_001269376.1:p.Leu622= | |
| NM_025220.5:c.1866G>T MANE Select | NP_079496.1:p.Leu622= | |
| NM_153202.4:c.1866G>T | NP_694882.1:p.Leu622= |