Linked Data
dbSNP Id:
rs762899172
ExAC:
6:76623911 G / A
gnomAD v2:
6-76623911-G-A
gnomAD v4:
6-75914194-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.75914194G>A , CM000668.2:g.75914194G>A | GRCh38 |
| NC_000006.11:g.76623911G>A , CM000668.1:g.76623911G>A | GRCh37 |
| NC_000006.10:g.76680631G>A | NCBI36 |
| NG_009934.1:g.170003G>A | |
| NG_009934.2:g.170002G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369975.6:c.3475G>A | ENSP00000358992.1:p.Gly1159Ser | |
| ENST00000369977.8:c.3571G>A MANE Select | ENSP00000358994.3:p.Gly1191Ser | |
| ENST00000369985.9:c.3502G>A | ENSP00000359002.3:p.Gly1168Ser | |
| ENST00000664640.1:c.3598G>A | ENSP00000499278.1:p.Gly1200Ser | |
| ENST00000671923.1:c.*1582G>A | ENSP00000500835.1:n.*1582G>A | |
| ENST00000672093.1:c.3571G>A | ENSP00000500710.1:p.Gly1191Ser | |
| ENST00000672162.1:n.1737G>A | ||
| ENST00000369975.5:c.3475G>A | ENSP00000358992.1:p.Gly1159Ser | |
| ENST00000369977.7:c.3571G>A | ENSP00000358994.3:p.Gly1191Ser | |
| ENST00000369981.7:c.3601G>A | ENSP00000358998.4:p.Gly1201Ser | |
| ENST00000369985.8:c.3502G>A | ENSP00000359002.3:p.Gly1168Ser | |
| ENST00000615563.4:c.3502G>A | ENSP00000478013.1:p.Gly1168Ser | |
| ENST00000627432.2:c.3598G>A | ENSP00000487348.1:p.Gly1200Ser | |
| NM_001300899.1:c.3502G>A | NP_001287828.1:p.Gly1168Ser | |
| NM_004999.3:c.3571G>A | NP_004990.3:p.Gly1191Ser | |
| XM_005248719.2:c.3598G>A | XP_005248776.1:p.Gly1200Ser | |
| XM_005248720.2:c.3571G>A | XP_005248777.1:p.Gly1191Ser | |
| XM_005248721.2:c.3559G>A | XP_005248778.1:p.Gly1187Ser | |
| XM_005248722.2:c.3544G>A | XP_005248779.1:p.Gly1182Ser | |
| XM_005248724.2:c.3532G>A | XP_005248781.1:p.Gly1178Ser | |
| XM_005248726.2:c.3475G>A | XP_005248783.1:p.Gly1159Ser | |
| XM_005248719.4:c.3598G>A | XP_005248776.1:p.Gly1200Ser | |
| XM_005248720.4:c.3571G>A | XP_005248777.1:p.Gly1191Ser | |
| XM_005248721.4:c.3559G>A | XP_005248778.1:p.Gly1187Ser | |
| XM_005248722.4:c.3544G>A | XP_005248779.1:p.Gly1182Ser | |
| XM_005248724.4:c.3532G>A | XP_005248781.1:p.Gly1178Ser | |
| XM_005248726.4:c.3475G>A | XP_005248783.1:p.Gly1159Ser | |
| XM_017010899.2:c.3505G>A | XP_016866388.1:p.Gly1169Ser | |
| XM_024446447.1:c.3598G>A | XP_024302215.1:p.Gly1200Ser | |
| XM_024446448.1:c.3532G>A | XP_024302216.1:p.Gly1178Ser | |
| NM_004999.4:c.3571G>A MANE Select | NP_004990.3:p.Gly1191Ser | |
| NM_001300899.2:c.3502G>A | NP_001287828.1:p.Gly1168Ser | |
| NM_001368136.1:c.3475G>A | NP_001355065.1:p.Gly1159Ser | |
| NM_001368137.1:c.3532G>A | NP_001355066.1:p.Gly1178Ser | |
| NM_001368138.1:c.3487G>A | NP_001355067.1:p.Gly1163Ser | |
| NM_001368865.1:c.3598G>A | NP_001355794.1:p.Gly1200Ser | |
| NM_001368866.1:c.3571G>A | NP_001355795.1:p.Gly1191Ser | |
| NR_160538.1:n.3800G>A |