Linked Data
dbSNP Id:
rs1400206687
gnomAD v2:
14-91739041-T-C
gnomAD v3:
14-91272697-T-C
gnomAD v4:
14-91272697-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.91272697T>C , CM000676.2:g.91272697T>C | GRCh38 |
| NC_000014.8:g.91739041T>C , CM000676.1:g.91739041T>C | GRCh37 |
| NC_000014.7:g.90808794T>C | NCBI36 |
| NG_033118.1:g.150148A>G | |
| NG_033118.2:g.150148A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000389857.11:c.6015A>G MANE Select | ENSP00000374507.6:p.Ser2005= | |
| ENST00000331194.8:c.1449A>G | ENSP00000330332.8:p.Ser483= | |
| ENST00000389857.10:c.6015A>G | ENSP00000374507.6:p.Ser2005= | |
| ENST00000556726.5:c.2243A>G | ||
| NM_001080414.3:c.6015A>G | NP_001073883.2:p.Ser2005= | |
| XM_011536796.1:c.5907A>G | XP_011535098.1:p.Ser1969= | |
| XM_011536796.2:c.5907A>G | XP_011535098.1:p.Ser1969= | |
| XM_017021336.1:c.3096A>G | XP_016876825.1:p.Ser1032= | |
| NM_001080414.4:c.6015A>G MANE Select | NP_001073883.2:p.Ser2005= |