Linked Data
gnomAD v4:
X-154928845-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154928845C>G , CM000685.2:g.154928845C>G | GRCh38 |
| NC_000023.10:g.154157120C>G , CM000685.1:g.154157120C>G | GRCh37 |
| NC_000023.9:g.153810314C>G | NCBI36 |
| NG_011403.1:g.98879G>C | |
| NG_011403.2:g.98879G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360256.9:c.4945G>C MANE Select | ENSP00000353393.4:p.Gly1649Arg | |
| ENST00000360256.8:c.4945G>C | ENSP00000353393.4:p.Gly1649Arg | |
| NM_000132.3:c.4945G>C | NP_000123.1:p.Gly1649Arg | |
| XM_011531126.1:c.4840G>C | XP_011529428.1:p.Gly1614Arg | |
| NM_000132.4:c.4945G>C MANE Select | NP_000123.1:p.Gly1649Arg |