Linked Data
MyVariant Identifiers:
chrX:g.154065998T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154837723T>A , CM000685.2:g.154837723T>A | GRCh38 |
| NC_000023.10:g.154065998T>A , CM000685.1:g.154065998T>A | GRCh37 |
| NC_000023.9:g.153719192T>A | NCBI36 |
| NG_011403.1:g.190001A>T | |
| NG_033065.1:g.1940A>T | |
| NG_011403.2:g.190001A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360256.9:c.6930A>T MANE Select | ENSP00000353393.4:p.Thr2310= | |
| ENST00000644698.1:c.663A>T | ENSP00000495706.1:p.Thr221= | |
| ENST00000330287.10:c.525A>T | ENSP00000327895.6:p.Thr175= | |
| ENST00000360256.8:c.6930A>T | ENSP00000353393.4:p.Thr2310= | |
| NM_000132.3:c.6930A>T | NP_000123.1:p.Thr2310= | |
| NM_019863.2:c.525A>T | NP_063916.1:p.Thr175= | |
| XM_011531126.1:c.6825A>T | XP_011529428.1:p.Thr2275= | |
| NM_000132.4:c.6930A>T MANE Select | NP_000123.1:p.Thr2310= | |
| NM_019863.3:c.525A>T | NP_063916.1:p.Thr175= |