Linked Data
gnomAD v4:
6-49447691-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.49447691C>A , CM000668.2:g.49447691C>A | GRCh38 |
| NC_000006.11:g.49415404C>A , CM000668.1:g.49415404C>A | GRCh37 |
| NC_000006.10:g.49523363C>A | NCBI36 |
| NG_007100.1:g.20449G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000274813.4:c.1539G>T MANE Select | ENSP00000274813.3:p.Arg513Ser | |
| ENST00000274813.3:c.1539G>T | ENSP00000274813.3:p.Arg513Ser | |
| NM_000255.3:c.1539G>T | NP_000246.2:p.Arg513Ser | |
| XM_005249143.2:c.1539G>T | XP_005249200.1:p.Arg513Ser | |
| XM_005249143.3:c.1539G>T | XP_005249200.1:p.Arg513Ser | |
| NM_000255.4:c.1539G>T MANE Select | NP_000246.2:p.Arg513Ser |