Linked Data
ClinVar Variation Id:
126421
dbSNP Id:
rs587777264
gnomAD v4:
9-135759686-G-A
PubMed:
PMID:24029078
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.135759686G>A , CM000671.2:g.135759686G>A | GRCh38 |
| NC_000009.11:g.138651532G>A , CM000671.1:g.138651532G>A | GRCh37 |
| NC_000009.10:g.137791353G>A | NCBI36 |
| NG_033070.1:g.62502G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000371757.7:c.862G>A MANE Select | ENSP00000360822.2:p.Gly288Ser | |
| ENST00000674572.1:c.703G>A | ENSP00000501742.1:p.Gly235Ser | |
| ENST00000675090.1:c.610G>A | ENSP00000501833.1:p.Gly204Ser | |
| ENST00000675399.1:c.610G>A | ENSP00000501932.1:p.Gly204Ser | |
| ENST00000676421.1:c.619G>A | ENSP00000502322.1:p.Gly207Ser | |
| ENST00000263604.5:c.763G>A | ENSP00000263604.4:p.Gly255Ser | |
| ENST00000371757.6:c.862G>A | ENSP00000360822.2:p.Gly288Ser | |
| ENST00000460750.5:c.*472G>A | ENSP00000418777.1:n.*472G>A | |
| ENST00000473941.5:c.703G>A | ENSP00000420764.1:p.Gly235Ser | |
| ENST00000486577.6:c.745G>A | ENSP00000417578.3:p.Gly249Ser | |
| ENST00000487664.5:c.862G>A | ENSP00000417851.2:p.Gly288Ser | |
| ENST00000488444.6:c.805G>A | ENSP00000419007.3:p.Gly269Ser | |
| ENST00000490355.6:c.805G>A | ENSP00000418003.3:p.Gly269Ser | |
| ENST00000490363.3:n.681G>A | ||
| ENST00000491806.6:c.805G>A | ENSP00000419086.3:p.Gly269Ser | |
| ENST00000628528.2:c.727G>A | ENSP00000486374.1:p.Gly243Ser | |
| ENST00000630792.2:c.703G>A | ENSP00000486486.1:p.Gly235Ser | |
| ENST00000631073.2:c.805G>A | ENSP00000486130.1:p.Gly269Ser | |
| NM_001272003.1:c.727G>A | NP_001258932.1:p.Gly243Ser | |
| NM_020822.2:c.862G>A | NP_065873.2:p.Gly288Ser | |
| XM_011518877.1:c.997G>A | XP_011517179.1:p.Gly333Ser | |
| XM_011518878.1:c.1006G>A | XP_011517180.1:p.Gly336Ser | |
| XM_011518879.1:c.997G>A | XP_011517181.1:p.Gly333Ser | |
| XM_011518880.1:c.763G>A | XP_011517182.1:p.Gly255Ser | |
| XM_011518881.1:c.352G>A | XP_011517183.1:p.Gly118Ser | |
| XM_011518877.3:c.997G>A | XP_011517179.1:p.Gly333Ser | |
| XM_011518878.3:c.1006G>A | XP_011517180.1:p.Gly336Ser | |
| XM_011518879.3:c.997G>A | XP_011517181.1:p.Gly333Ser | |
| XM_011518881.3:c.352G>A | XP_011517183.1:p.Gly118Ser | |
| XM_017014931.1:c.796G>A | XP_016870420.1:p.Gly266Ser | |
| XM_017014932.1:c.619G>A | XP_016870421.1:p.Gly207Ser | |
| XM_017014933.1:c.352G>A | XP_016870422.1:p.Gly118Ser | |
| XM_024447617.1:c.352G>A | XP_024303385.1:p.Gly118Ser | |
| XM_024447618.1:c.352G>A | XP_024303386.1:p.Gly118Ser | |
| NM_020822.3:c.862G>A MANE Select | NP_065873.2:p.Gly288Ser | |
| NM_001272003.2:c.727G>A | NP_001258932.1:p.Gly243Ser |