Linked Data
gnomAD v4:
14-21312443-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.21312443G>C , CM000676.2:g.21312443G>C | GRCh38 |
| NC_000014.8:g.21780602G>C , CM000676.1:g.21780602G>C | GRCh37 |
| NC_000014.7:g.20850442G>C | NCBI36 |
| NG_008933.1:g.29467G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000400017.7:c.1088G>C MANE Select | ENSP00000382895.2:p.Arg363Thr | |
| ENST00000400017.6:c.1088G>C | ENSP00000382895.2:p.Arg363Thr | |
| ENST00000556336.5:c.1007G>C | ENSP00000450445.1:p.Arg336Thr | |
| ENST00000557771.5:c.1007G>C | ENSP00000451219.1:p.Arg336Thr | |
| NM_020366.3:c.1088G>C | NP_065099.3:p.Arg363Thr | |
| XM_011536983.1:c.1055G>C | XP_011535285.1:p.Arg352Thr | |
| NM_020366.4:c.1088G>C MANE Select | NP_065099.3:p.Arg363Thr |