Linked Data
gnomAD v4:
4-47406896-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.47406896G>T , CM000666.2:g.47406896G>T | GRCh38 |
| NC_000004.11:g.47408913G>T , CM000666.1:g.47408913G>T | GRCh37 |
| NC_000004.10:g.47103670G>T | NCBI36 |
| NG_051831.1:g.380619G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000295454.8:c.1050G>T MANE Select | ENSP00000295454.3:p.Glu350Asp | |
| ENST00000295454.7:c.1050G>T | ENSP00000295454.3:p.Glu350Asp | |
| NM_000812.3:c.1050G>T | NP_000803.2:p.Glu350Asp | |
| XM_011513678.1:c.1029G>T | XP_011511980.1:p.Glu343Asp | |
| XM_017007985.1:c.399G>T | XP_016863474.1:p.Glu133Asp | |
| XM_024453976.1:c.951G>T | XP_024309744.1:p.Glu317Asp | |
| XM_024453977.1:c.951G>T | XP_024309745.1:p.Glu317Asp | |
| XM_024453978.1:c.951G>T | XP_024309746.1:p.Glu317Asp | |
| NM_000812.4:c.1050G>T MANE Select | NP_000803.2:p.Glu350Asp |