Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.91272802C>T , CM000676.2:g.91272802C>T | GRCh38 |
| NC_000014.8:g.91739146C>T , CM000676.1:g.91739146C>T | GRCh37 |
| NC_000014.7:g.90808899C>T | NCBI36 |
| NG_033118.1:g.150043G>A | |
| NG_033118.2:g.150043G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000389857.11:c.5910G>A MANE Select | ENSP00000374507.6:p.Gly1970= | |
| ENST00000331194.8:c.1344G>A | ENSP00000330332.8:p.Gly448= | |
| ENST00000389857.10:c.5910G>A | ENSP00000374507.6:p.Gly1970= | |
| ENST00000556726.5:c.2138G>A | ||
| NM_001080414.3:c.5910G>A | NP_001073883.2:p.Gly1970= | |
| XM_011536796.1:c.5802G>A | XP_011535098.1:p.Gly1934= | |
| XM_011536796.2:c.5802G>A | XP_011535098.1:p.Gly1934= | |
| XM_017021336.1:c.2991G>A | XP_016876825.1:p.Gly997= | |
| NM_001080414.4:c.5910G>A MANE Select | NP_001073883.2:p.Gly1970= |