Linked Data
ClinVar Variation Id:
127291
dbSNP Id:
rs587779791
ExAC:
5:112175226 G / C
gnomAD v2:
5-112175226-G-C
gnomAD v4:
5-112839529-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.112839529G>C , CM000667.2:g.112839529G>C | GRCh38 |
| NC_000005.9:g.112175226G>C , CM000667.1:g.112175226G>C | GRCh37 |
| NC_000005.8:g.112203125G>C | NCBI36 |
| NG_008481.4:g.152009G>C , LRG_130:g.152009G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000502371.3:c.3600G>C | ENSP00000484935.2:n.3600G>C | |
| ENST00000504915.3:c.3989G>C | ENSP00000473355.2:p.Gly1330Ala | |
| ENST00000505350.2:c.*3941G>C | ENSP00000481752.1:n.*3941G>C | |
| ENST00000507379.6:c.3881G>C | ENSP00000423224.2:p.Gly1294Ala | |
| ENST00000509732.6:c.3935G>C | ENSP00000426541.2:p.Gly1312Ala | |
| ENST00000512211.7:c.3935G>C | ENSP00000423828.3:p.Gly1312Ala | |
| ENST00000257430.9:c.3935G>C MANE Select | ENSP00000257430.4:p.Gly1312Ala | |
| ENST00000257430.8:c.3935G>C | ENSP00000257430.4:p.Gly1312Ala | |
| ENST00000502371.2:c.2288G>C | ||
| ENST00000508376.6:c.3935G>C | ENSP00000427089.2:p.Gly1312Ala | |
| ENST00000508624.5:c.*3257G>C | ENSP00000424265.1:n.*3257G>C | |
| ENST00000520401.1:c.230+10557G>C | ||
| NM_000038.5:c.3935G>C | NP_000029.2:p.Gly1312Ala | |
| NM_001127510.2:c.3935G>C | NP_001120982.1:p.Gly1312Ala | |
| NM_001127511.2:c.3881G>C | NP_001120983.2:p.Gly1294Ala | |
| NM_001354895.1:c.3935G>C | NP_001341824.1:p.Gly1312Ala | |
| NM_001354896.1:c.3989G>C | NP_001341825.1:p.Gly1330Ala | |
| NM_001354897.1:c.3965G>C | NP_001341826.1:p.Gly1322Ala | |
| NM_001354898.1:c.3860G>C | NP_001341827.1:p.Gly1287Ala | |
| NM_001354899.1:c.3851G>C | NP_001341828.1:p.Gly1284Ala | |
| NM_001354900.1:c.3812G>C | NP_001341829.1:p.Gly1271Ala | |
| NM_001354901.1:c.3758G>C | NP_001341830.1:p.Gly1253Ala | |
| NM_001354902.1:c.3662G>C | NP_001341831.1:p.Gly1221Ala | |
| NM_001354903.1:c.3632G>C | NP_001341832.1:p.Gly1211Ala | |
| NM_001354904.1:c.3557G>C | NP_001341833.1:p.Gly1186Ala | |
| NM_001354905.1:c.3455G>C | NP_001341834.1:p.Gly1152Ala | |
| NM_001354906.1:c.3086G>C | NP_001341835.1:p.Gly1029Ala | |
| NM_000038.6:c.3935G>C MANE Select | NP_000029.2:p.Gly1312Ala | |
| NM_001127510.3:c.3935G>C | NP_001120982.1:p.Gly1312Ala | |
| NM_001127511.3:c.3881G>C | NP_001120983.2:p.Gly1294Ala | |
| NM_001354895.2:c.3935G>C | NP_001341824.1:p.Gly1312Ala | |
| NM_001354896.2:c.3989G>C | NP_001341825.1:p.Gly1330Ala | |
| NM_001354897.2:c.3965G>C | NP_001341826.1:p.Gly1322Ala | |
| NM_001354898.2:c.3860G>C | NP_001341827.1:p.Gly1287Ala | |
| NM_001354899.2:c.3851G>C | NP_001341828.1:p.Gly1284Ala | |
| NM_001354900.2:c.3812G>C | NP_001341829.1:p.Gly1271Ala | |
| NM_001354901.2:c.3758G>C | NP_001341830.1:p.Gly1253Ala | |
| NM_001354902.2:c.3662G>C | NP_001341831.1:p.Gly1221Ala | |
| NM_001354903.2:c.3632G>C | NP_001341832.1:p.Gly1211Ala | |
| NM_001354904.2:c.3557G>C | NP_001341833.1:p.Gly1186Ala | |
| NM_001354905.2:c.3455G>C | NP_001341834.1:p.Gly1152Ala | |
| NM_001354906.2:c.3086G>C | NP_001341835.1:p.Gly1029Ala |