Linked Data
MyVariant Identifiers:
chr14:g.91739053T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.91272709T>G , CM000676.2:g.91272709T>G | GRCh38 |
| NC_000014.8:g.91739053T>G , CM000676.1:g.91739053T>G | GRCh37 |
| NC_000014.7:g.90808806T>G | NCBI36 |
| NG_033118.1:g.150136A>C | |
| NG_033118.2:g.150136A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000389857.11:c.6003A>C MANE Select | ENSP00000374507.6:p.Arg2001= | |
| ENST00000331194.8:c.1437A>C | ENSP00000330332.8:p.Arg479= | |
| ENST00000389857.10:c.6003A>C | ENSP00000374507.6:p.Arg2001= | |
| ENST00000556726.5:c.2231A>C | ||
| NM_001080414.3:c.6003A>C | NP_001073883.2:p.Arg2001= | |
| XM_011536796.1:c.5895A>C | XP_011535098.1:p.Arg1965= | |
| XM_011536796.2:c.5895A>C | XP_011535098.1:p.Arg1965= | |
| XM_017021336.1:c.3084A>C | XP_016876825.1:p.Arg1028= | |
| NM_001080414.4:c.6003A>C MANE Select | NP_001073883.2:p.Arg2001= |