Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.47406864G>A , CM000666.2:g.47406864G>A | GRCh38 |
| NC_000004.11:g.47408881G>A , CM000666.1:g.47408881G>A | GRCh37 |
| NC_000004.10:g.47103638G>A | NCBI36 |
| NG_051831.1:g.380587G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000295454.8:c.1018G>A MANE Select | ENSP00000295454.3:p.Gly340Arg | |
| ENST00000295454.7:c.1018G>A | ENSP00000295454.3:p.Gly340Arg | |
| NM_000812.3:c.1018G>A | NP_000803.2:p.Gly340Arg | |
| XM_011513678.1:c.997G>A | XP_011511980.1:p.Gly333Arg | |
| XM_017007985.1:c.367G>A | XP_016863474.1:p.Gly123Arg | |
| XM_024453976.1:c.919G>A | XP_024309744.1:p.Gly307Arg | |
| XM_024453977.1:c.919G>A | XP_024309745.1:p.Gly307Arg | |
| XM_024453978.1:c.919G>A | XP_024309746.1:p.Gly307Arg | |
| NM_000812.4:c.1018G>A MANE Select | NP_000803.2:p.Gly340Arg |