Linked Data
MyVariant Identifiers:
chrX:g.154157064C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154928789C>A , CM000685.2:g.154928789C>A | GRCh38 |
| NC_000023.10:g.154157064C>A , CM000685.1:g.154157064C>A | GRCh37 |
| NC_000023.9:g.153810258C>A | NCBI36 |
| NG_011403.1:g.98935G>T | |
| NG_011403.2:g.98935G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360256.9:c.5001G>T MANE Select | ENSP00000353393.4:p.Arg1667= | |
| ENST00000360256.8:c.5001G>T | ENSP00000353393.4:p.Arg1667= | |
| NM_000132.3:c.5001G>T | NP_000123.1:p.Arg1667= | |
| XM_011531126.1:c.4896G>T | XP_011529428.1:p.Arg1632= | |
| NM_000132.4:c.5001G>T MANE Select | NP_000123.1:p.Arg1667= |