Linked Data
ClinVar Variation Id:
310900
ClinVar RCV Id:
RCV000376429
dbSNP Id:
rs776794756
ExAC:
13:102379092 G / A
gnomAD v2:
13-102379092-G-A
gnomAD v4:
13-101726742-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.101726742G>A , CM000675.2:g.101726742G>A | GRCh38 |
| NC_000013.10:g.102379092G>A , CM000675.1:g.102379092G>A | GRCh37 |
| NC_000013.9:g.101177093G>A | NCBI36 |
| NG_008317.1:g.680033C>T | |
| NG_008317.2:g.680033C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000376131.9:c.492C>T | ENSP00000365301.3:p.Ser164= | |
| ENST00000418923.3:c.375C>T | ENSP00000516414.1:p.Ser125= | |
| ENST00000706491.1:c.*81C>T | ENSP00000516413.1:n.*81C>T | |
| ENST00000706492.1:c.*296C>T | ENSP00000516415.1:n.*296C>T | |
| ENST00000706493.1:c.*391C>T | ENSP00000516416.1:n.*391C>T | |
| ENST00000706494.1:c.225C>T | ENSP00000516417.1:p.Ser75= | |
| ENST00000376143.5:c.477C>T MANE Select | ENSP00000365313.4:p.Ser159= | |
| ENST00000376131.8:c.492C>T | ENSP00000365301.3:p.Ser164= | |
| ENST00000376143.4:c.477C>T | ENSP00000365313.4:p.Ser159= | |
| NM_004115.3:c.477C>T | NP_004106.1:p.Ser159= | |
| NM_175929.2:c.492C>T | NP_787125.1:p.Ser164= | |
| XM_011521053.1:c.297C>T | XP_011519355.1:p.Ser99= | |
| NM_001321931.1:c.225C>T | NP_001308860.1:p.Ser75= | |
| NM_001321932.1:c.288C>T | NP_001308861.1:p.Ser96= | |
| NM_001321933.1:c.297C>T | NP_001308862.1:p.Ser99= | |
| NM_001321934.1:c.225C>T | NP_001308863.1:p.Ser75= | |
| NM_001321935.1:c.225C>T | NP_001308864.1:p.Ser75= | |
| NM_001321936.1:c.288C>T | NP_001308865.1:p.Ser96= | |
| NM_001321938.1:c.297C>T | NP_001308867.1:p.Ser99= | |
| NM_001321939.1:c.381C>T | NP_001308868.1:p.Ser127= | |
| NM_001321940.1:c.297C>T | NP_001308869.1:p.Ser99= | |
| NM_001321941.1:c.291C>T | NP_001308870.1:p.Ser97= | |
| NM_001321942.1:c.225C>T | NP_001308871.1:p.Ser75= | |
| NM_001321943.1:c.225C>T | NP_001308872.1:p.Ser75= | |
| NM_001321944.1:c.288C>T | NP_001308873.1:p.Ser96= | |
| NM_001321945.1:c.375C>T | NP_001308874.1:p.Ser125= | |
| NM_001321946.1:c.225C>T | NP_001308875.1:p.Ser75= | |
| NM_001321947.1:c.336C>T | NP_001308876.1:p.Ser112= | |
| NM_001321948.1:c.375C>T | NP_001308877.1:p.Ser125= | |
| NM_001321949.1:c.225C>T | NP_001308878.1:p.Ser75= | |
| NM_001321938.2:c.297C>T | NP_001308867.1:p.Ser99= | |
| NM_001321945.2:c.375C>T | NP_001308874.1:p.Ser125= | |
| NM_001321946.2:c.225C>T | NP_001308875.1:p.Ser75= | |
| NM_001321947.2:c.336C>T | NP_001308876.1:p.Ser112= | |
| NM_001321948.2:c.375C>T | NP_001308877.1:p.Ser125= | |
| NM_001321939.2:c.381C>T | NP_001308868.1:p.Ser127= | |
| NM_001321941.2:c.291C>T | NP_001308870.1:p.Ser97= | |
| NM_001379342.1:c.375C>T | NP_001366271.1:p.Ser125= | |
| NM_004115.4:c.477C>T MANE Select | NP_004106.1:p.Ser159= | |
| NM_175929.3:c.492C>T | NP_787125.1:p.Ser164= |