Linked Data
ClinVar Variation Id:
2528992
ClinVar RCV Id:
RCV003242218
gnomAD v4:
18-33744544-C-T
COSMIC:
COSM987938
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.33744544C>T , CM000680.2:g.33744544C>T | GRCh38 |
| NC_000018.9:g.31324508C>T , CM000680.1:g.31324508C>T | GRCh37 |
| NC_000018.8:g.29578506C>T | NCBI36 |
| NG_055244.1:g.170968C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696964.1:c.4699C>T | ENSP00000513003.1:p.Pro1567Ser | |
| ENST00000269197.12:c.4696C>T MANE Select | ENSP00000269197.4:p.Pro1566Ser | |
| ENST00000681521.1:c.4576C>T | ENSP00000506037.1:p.Pro1526Ser | |
| ENST00000269197.9:c.4696C>T | ENSP00000269197.4:p.Pro1566Ser | |
| NM_030632.1:c.4696C>T | NP_085135.1:p.Pro1566Ser | |
| XM_005258356.1:c.4699C>T | XP_005258413.1:p.Pro1567Ser | |
| XM_011526205.1:c.4672C>T | XP_011524507.1:p.Pro1558Ser | |
| XM_011526206.1:c.4618C>T | XP_011524508.1:p.Pro1540Ser | |
| XM_011526207.1:c.4618C>T | XP_011524509.1:p.Pro1540Ser | |
| XM_011526208.1:c.4579C>T | XP_011524510.1:p.Pro1527Ser | |
| XM_011526209.1:c.4528C>T | XP_011524511.1:p.Pro1510Ser | |
| XM_011526210.1:c.4528C>T | XP_011524512.1:p.Pro1510Ser | |
| XM_011526211.1:c.4528C>T | XP_011524513.1:p.Pro1510Ser | |
| XM_011526212.1:c.4528C>T | XP_011524514.1:p.Pro1510Ser | |
| XM_011526213.1:c.4528C>T | XP_011524515.1:p.Pro1510Ser | |
| XM_011526214.1:c.4528C>T | XP_011524516.1:p.Pro1510Ser | |
| XM_011526215.1:c.1660C>T | XP_011524517.1:p.Pro554Ser | |
| NM_030632.2:c.4696C>T | NP_085135.1:p.Pro1566Ser | |
| XM_011526205.2:c.4672C>T | XP_011524507.1:p.Pro1558Ser | |
| XM_011526206.2:c.4618C>T | XP_011524508.1:p.Pro1540Ser | |
| XM_011526213.2:c.4528C>T | XP_011524515.1:p.Pro1510Ser | |
| XM_017026012.1:c.4618C>T | XP_016881501.1:p.Pro1540Ser | |
| XM_017026013.1:c.4528C>T | XP_016881502.1:p.Pro1510Ser | |
| XM_017026014.2:c.4528C>T | XP_016881503.1:p.Pro1510Ser | |
| XM_024451269.1:c.4528C>T | XP_024307037.1:p.Pro1510Ser | |
| NM_030632.3:c.4696C>T MANE Select | NP_085135.1:p.Pro1566Ser |