Linked Data
dbSNP Id:
rs773030985
ExAC:
5:180036970 C / T
gnomAD v2:
5-180036970-C-T
gnomAD v3:
5-180609970-C-T
gnomAD v4:
5-180609970-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.180609970C>T , CM000667.2:g.180609970C>T | GRCh38 |
| NC_000005.9:g.180036970C>T , CM000667.1:g.180036970C>T | GRCh37 |
| NC_000005.8:g.179969576C>T | NCBI36 |
| NG_011536.1:g.44655G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261937.11:c.3742G>A MANE Select | ENSP00000261937.6:p.Gly1248Ser | |
| ENST00000261937.10:c.3742G>A | ENSP00000261937.6:p.Gly1248Ser | |
| ENST00000393347.7:c.3742G>A | ENSP00000377016.3:p.Gly1248Ser | |
| ENST00000502603.5:n.442G>A | ||
| ENST00000502649.5:c.3742G>A | ENSP00000426057.1:p.Gly1248Ser | |
| ENST00000507059.5:n.4092G>A | ||
| ENST00000619105.4:c.*2685G>A | ENSP00000481134.1:n.*2685G>A | |
| NM_002020.4:c.3742G>A | NP_002011.2:p.Gly1248Ser | |
| NM_182925.4:c.3742G>A | NP_891555.2:p.Gly1248Ser | |
| XM_011534477.1:c.3991G>A | XP_011532779.1:p.Gly1331Ser | |
| XM_011534478.1:c.3973G>A | XP_011532780.1:p.Gly1325Ser | |
| XM_011534479.1:c.3991G>A | XP_011532781.1:p.Gly1331Ser | |
| XM_011534480.1:c.3991G>A | XP_011532782.1:p.Gly1331Ser | |
| XM_011534481.1:c.3991G>A | XP_011532783.1:p.Gly1331Ser | |
| XM_011534482.1:c.3760G>A | XP_011532784.1:p.Gly1254Ser | |
| XM_011534483.1:c.3682G>A | XP_011532785.1:p.Gly1228Ser | |
| XM_011534484.1:c.3283G>A | XP_011532786.1:p.Gly1095Ser | |
| XR_941095.1:n.4028G>A | ||
| NM_001354989.1:c.3742G>A | NP_001341918.1:p.Gly1248Ser | |
| XM_011534478.3:c.3973G>A | XP_011532780.1:p.Gly1325Ser | |
| XM_011534484.2:c.3283G>A | XP_011532786.1:p.Gly1095Ser | |
| XM_017009263.1:c.3973G>A | XP_016864752.1:p.Gly1325Ser | |
| XM_017009264.2:c.3973G>A | XP_016864753.1:p.Gly1325Ser | |
| XM_017009265.1:c.3973G>A | XP_016864754.1:p.Gly1325Ser | |
| XM_017009266.1:c.3973G>A | XP_016864755.1:p.Gly1325Ser | |
| XM_017009267.2:c.3973G>A | XP_016864756.1:p.Gly1325Ser | |
| XM_017009268.1:c.3664G>A | XP_016864757.1:p.Gly1222Ser | |
| XR_001742050.2:n.4232G>A | ||
| NM_182925.5:c.3742G>A MANE Select | NP_891555.2:p.Gly1248Ser | |
| NM_001354989.2:c.3742G>A | NP_001341918.1:p.Gly1248Ser | |
| NM_002020.5:c.3742G>A | NP_002011.2:p.Gly1248Ser |