Linked Data
MyVariant Identifiers:
chr14:g.91739185C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.91272841C>G , CM000676.2:g.91272841C>G | GRCh38 |
| NC_000014.8:g.91739185C>G , CM000676.1:g.91739185C>G | GRCh37 |
| NC_000014.7:g.90808938C>G | NCBI36 |
| NG_033118.1:g.150004G>C | |
| NG_033118.2:g.150004G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000389857.11:c.5871G>C MANE Select | ENSP00000374507.6:p.Arg1957= | |
| ENST00000331194.8:c.1305G>C | ENSP00000330332.8:p.Arg435= | |
| ENST00000389857.10:c.5871G>C | ENSP00000374507.6:p.Arg1957= | |
| ENST00000556726.5:c.2099G>C | ||
| NM_001080414.3:c.5871G>C | NP_001073883.2:p.Arg1957= | |
| XM_011536796.1:c.5763G>C | XP_011535098.1:p.Arg1921= | |
| XM_011536796.2:c.5763G>C | XP_011535098.1:p.Arg1921= | |
| XM_017021336.1:c.2952G>C | XP_016876825.1:p.Arg984= | |
| NM_001080414.4:c.5871G>C MANE Select | NP_001073883.2:p.Arg1957= |