Linked Data
ClinVar Variation Id:
329517
dbSNP Id:
rs146022050
ExAC:
19:45867131 G / A
gnomAD v2:
19-45867131-G-A
gnomAD v3:
19-45363873-G-A
gnomAD v4:
19-45363873-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.45363873G>A , CM000681.2:g.45363873G>A | GRCh38 |
| NC_000019.9:g.45867131G>A , CM000681.1:g.45867131G>A | GRCh37 |
| NC_000019.8:g.50558971G>A | NCBI36 |
| NG_007067.2:g.11715C>T , LRG_461:g.11715C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000391944.8:c.988C>T | ENSP00000375808.4:p.Leu330= | |
| ENST00000682414.1:c.988C>T | ENSP00000507019.1:p.Leu330= | |
| ENST00000682508.1:n.1017C>T | ||
| ENST00000684218.1:c.*246C>T | ENSP00000507804.1:n.*246C>T | |
| ENST00000684407.1:c.865C>T | ENSP00000507775.1:p.Leu289= | |
| ENST00000684458.1:c.988C>T | ENSP00000508260.1:p.Leu330= | |
| ENST00000391945.10:c.988C>T MANE Select | ENSP00000375809.4:p.Leu330= | |
| ENST00000587376.6:c.111C>T | ||
| ENST00000646507.1:n.1085C>T | ||
| ENST00000391941.6:c.916C>T | ENSP00000375805.2:p.Leu306= | |
| ENST00000391944.7:c.754C>T | ENSP00000375808.3:p.Leu252= | |
| ENST00000391945.8:c.988C>T | ENSP00000375809.3:p.Leu330= | |
| ENST00000485403.6:c.916C>T | ENSP00000431229.2:p.Leu306= | |
| ENST00000587376.5:c.111C>T | ||
| NM_000400.3:c.988C>T , LRG_461t1:c.988C>T | NP_000391.1:p.Leu330= | |
| NM_001130867.1:c.916C>T | NP_001124339.1:p.Leu306= | |
| XM_011526611.1:c.910C>T | XP_011524913.1:p.Leu304= | |
| XR_935763.1:n.1035C>T | ||
| XM_011526611.2:c.910C>T | XP_011524913.1:p.Leu304= | |
| XM_017026467.1:c.865C>T | XP_016881956.1:p.Leu289= | |
| XR_001753633.2:n.1035C>T | ||
| XR_001753634.2:n.1035C>T | ||
| NM_000400.4:c.988C>T MANE Select | NP_000391.1:p.Leu330= | |
| NM_001130867.2:c.916C>T | NP_001124339.1:p.Leu306= |