Linked Data
ClinVar Variation Id:
2945240
ClinVar RCV Id:
RCV003800894
MyVariant Identifiers:
chr1:g.197390347C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.197421217C>G , CM000663.2:g.197421217C>G | GRCh38 |
| NC_000001.10:g.197390347C>G , CM000663.1:g.197390347C>G | GRCh37 |
| NC_000001.9:g.195656970C>G | NCBI36 |
| NG_008483.1:g.157940C>G | |
| NG_008483.2:g.224756C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367400.8:c.1389C>G MANE Select | ENSP00000356370.3:p.Gly463= | |
| ENST00000638467.1:c.1389C>G | ENSP00000491102.1:p.Gly463= | |
| ENST00000681519.1:c.270C>G | ENSP00000505267.1:p.Gly90= | |
| ENST00000367397.1:c.-469C>G | ENSP00000356367.1:n.-469C>G | |
| ENST00000367399.6:c.1053C>G | ENSP00000356369.2:p.Gly351= | |
| ENST00000367400.7:c.1389C>G | ENSP00000356370.3:p.Gly463= | |
| ENST00000476483.1:n.349C>G | ||
| ENST00000484075.5:c.1389C>G | ENSP00000433932.1:p.Gly463= | |
| ENST00000535699.5:c.1182C>G | ENSP00000438786.1:p.Gly394= | |
| ENST00000538660.5:c.1389C>G | ENSP00000438091.1:p.Gly463= | |
| NM_001193640.1:c.1053C>G | NP_001180569.1:p.Gly351= | |
| NM_001257965.1:c.1182C>G | NP_001244894.1:p.Gly394= | |
| NM_001257966.1:c.1389C>G | NP_001244895.1:p.Gly463= | |
| NM_201253.2:c.1389C>G | NP_957705.1:p.Gly463= | |
| NR_047563.1:n.1598C>G | ||
| NR_047564.1:n.1598C>G | ||
| XM_011509365.1:c.1389C>G | XP_011507667.1:p.Gly463= | |
| XM_011509366.1:c.1389C>G | XP_011507668.1:p.Gly463= | |
| XM_011509367.1:c.1389C>G | XP_011507669.1:p.Gly463= | |
| XM_011509368.1:c.807C>G | XP_011507670.1:p.Gly269= | |
| XM_011509369.1:c.-169C>G | XP_011507671.1:n.-169C>G | |
| XM_011509365.2:c.1389C>G | XP_011507667.1:p.Gly463= | |
| XM_011509369.2:c.-169C>G | XP_011507671.1:n.-169C>G | |
| XM_017000851.1:c.546C>G | XP_016856340.1:p.Gly182= | |
| XM_017000852.1:c.1389C>G | XP_016856341.1:p.Gly463= | |
| NM_201253.3:c.1389C>G MANE Select | NP_957705.1:p.Gly463= | |
| NM_001193640.2:c.1053C>G | NP_001180569.1:p.Gly351= | |
| NM_001257965.2:c.1182C>G | NP_001244894.1:p.Gly394= | |
| NR_047563.2:n.1550C>G | ||
| NR_047564.2:n.1550C>G | ||
| NM_001257966.2:c.1389C>G | NP_001244895.1:p.Gly463= |