Linked Data
dbSNP Id:
rs775580963
ExAC:
5:180040063 G / T
gnomAD v2:
5-180040063-G-T
gnomAD v3:
5-180613063-G-T
gnomAD v4:
5-180613063-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.180613063G>T , CM000667.2:g.180613063G>T | GRCh38 |
| NC_000005.9:g.180040063G>T , CM000667.1:g.180040063G>T | GRCh37 |
| NC_000005.8:g.179972669G>T | NCBI36 |
| NG_011536.1:g.41562C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261937.11:c.3379C>A MANE Select | ENSP00000261937.6:p.Arg1127= | |
| ENST00000261937.10:c.3379C>A | ENSP00000261937.6:p.Arg1127= | |
| ENST00000393347.7:c.3379C>A | ENSP00000377016.3:p.Arg1127= | |
| ENST00000502649.5:c.3379C>A | ENSP00000426057.1:p.Arg1127= | |
| ENST00000507059.5:n.3729C>A | ||
| ENST00000510000.1:n.331C>A | ||
| ENST00000619105.4:c.*2322C>A | ENSP00000481134.1:n.*2322C>A | |
| NM_002020.4:c.3379C>A | NP_002011.2:p.Arg1127= | |
| NM_182925.4:c.3379C>A | NP_891555.2:p.Arg1127= | |
| XM_011534477.1:c.3628C>A | XP_011532779.1:p.Arg1210= | |
| XM_011534478.1:c.3610C>A | XP_011532780.1:p.Arg1204= | |
| XM_011534479.1:c.3628C>A | XP_011532781.1:p.Arg1210= | |
| XM_011534480.1:c.3628C>A | XP_011532782.1:p.Arg1210= | |
| XM_011534481.1:c.3628C>A | XP_011532783.1:p.Arg1210= | |
| XM_011534482.1:c.3397C>A | XP_011532784.1:p.Arg1133= | |
| XM_011534483.1:c.3319C>A | XP_011532785.1:p.Arg1107= | |
| XM_011534484.1:c.2920C>A | XP_011532786.1:p.Arg974= | |
| XR_941095.1:n.3640C>A | ||
| NM_001354989.1:c.3379C>A | NP_001341918.1:p.Arg1127= | |
| XM_011534478.3:c.3610C>A | XP_011532780.1:p.Arg1204= | |
| XM_011534484.2:c.2920C>A | XP_011532786.1:p.Arg974= | |
| XM_017009263.1:c.3610C>A | XP_016864752.1:p.Arg1204= | |
| XM_017009264.2:c.3610C>A | XP_016864753.1:p.Arg1204= | |
| XM_017009265.1:c.3610C>A | XP_016864754.1:p.Arg1204= | |
| XM_017009266.1:c.3610C>A | XP_016864755.1:p.Arg1204= | |
| XM_017009267.2:c.3610C>A | XP_016864756.1:p.Arg1204= | |
| XM_017009268.1:c.3301C>A | XP_016864757.1:p.Arg1101= | |
| XR_001742050.2:n.3844C>A | ||
| NM_182925.5:c.3379C>A MANE Select | NP_891555.2:p.Arg1127= | |
| NM_001354989.2:c.3379C>A | NP_001341918.1:p.Arg1127= | |
| NM_002020.5:c.3379C>A | NP_002011.2:p.Arg1127= |