Linked Data
dbSNP Id:
rs2035465308
gnomAD v3:
13-101726772-A-C
gnomAD v4:
13-101726772-A-C
MyVariant Identifiers:
chr13:g.102379122A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.101726772A>C , CM000675.2:g.101726772A>C | GRCh38 |
| NC_000013.10:g.102379122A>C , CM000675.1:g.102379122A>C | GRCh37 |
| NC_000013.9:g.101177123A>C | NCBI36 |
| NG_008317.1:g.680003T>G | |
| NG_008317.2:g.680003T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000376131.9:c.462T>G | ENSP00000365301.3:p.Val154= | |
| ENST00000418923.3:c.345T>G | ENSP00000516414.1:p.Val115= | |
| ENST00000706491.1:c.*51T>G | ENSP00000516413.1:n.*51T>G | |
| ENST00000706492.1:c.*266T>G | ENSP00000516415.1:n.*266T>G | |
| ENST00000706493.1:c.*361T>G | ENSP00000516416.1:n.*361T>G | |
| ENST00000706494.1:c.195T>G | ENSP00000516417.1:p.Val65= | |
| ENST00000376143.5:c.447T>G MANE Select | ENSP00000365313.4:p.Val149= | |
| ENST00000376131.8:c.462T>G | ENSP00000365301.3:p.Val154= | |
| ENST00000376143.4:c.447T>G | ENSP00000365313.4:p.Val149= | |
| NM_004115.3:c.447T>G | NP_004106.1:p.Val149= | |
| NM_175929.2:c.462T>G | NP_787125.1:p.Val154= | |
| XM_011521053.1:c.267T>G | XP_011519355.1:p.Val89= | |
| NM_001321931.1:c.195T>G | NP_001308860.1:p.Val65= | |
| NM_001321932.1:c.258T>G | NP_001308861.1:p.Val86= | |
| NM_001321933.1:c.267T>G | NP_001308862.1:p.Val89= | |
| NM_001321934.1:c.195T>G | NP_001308863.1:p.Val65= | |
| NM_001321935.1:c.195T>G | NP_001308864.1:p.Val65= | |
| NM_001321936.1:c.258T>G | NP_001308865.1:p.Val86= | |
| NM_001321938.1:c.267T>G | NP_001308867.1:p.Val89= | |
| NM_001321939.1:c.351T>G | NP_001308868.1:p.Val117= | |
| NM_001321940.1:c.267T>G | NP_001308869.1:p.Val89= | |
| NM_001321941.1:c.261T>G | NP_001308870.1:p.Val87= | |
| NM_001321942.1:c.195T>G | NP_001308871.1:p.Val65= | |
| NM_001321943.1:c.195T>G | NP_001308872.1:p.Val65= | |
| NM_001321944.1:c.258T>G | NP_001308873.1:p.Val86= | |
| NM_001321945.1:c.345T>G | NP_001308874.1:p.Val115= | |
| NM_001321946.1:c.195T>G | NP_001308875.1:p.Val65= | |
| NM_001321947.1:c.306T>G | NP_001308876.1:p.Val102= | |
| NM_001321948.1:c.345T>G | NP_001308877.1:p.Val115= | |
| NM_001321949.1:c.195T>G | NP_001308878.1:p.Val65= | |
| NM_001321938.2:c.267T>G | NP_001308867.1:p.Val89= | |
| NM_001321945.2:c.345T>G | NP_001308874.1:p.Val115= | |
| NM_001321946.2:c.195T>G | NP_001308875.1:p.Val65= | |
| NM_001321947.2:c.306T>G | NP_001308876.1:p.Val102= | |
| NM_001321948.2:c.345T>G | NP_001308877.1:p.Val115= | |
| NM_001321939.2:c.351T>G | NP_001308868.1:p.Val117= | |
| NM_001321941.2:c.261T>G | NP_001308870.1:p.Val87= | |
| NM_001379342.1:c.345T>G | NP_001366271.1:p.Val115= | |
| NM_004115.4:c.447T>G MANE Select | NP_004106.1:p.Val149= | |
| NM_175929.3:c.462T>G | NP_787125.1:p.Val154= |