Linked Data
MyVariant Identifiers:
chrX:g.154091443A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154863168A>T , CM000685.2:g.154863168A>T | GRCh38 |
| NC_000023.10:g.154091443A>T , CM000685.1:g.154091443A>T | GRCh37 |
| NC_000023.9:g.153744637A>T | NCBI36 |
| NG_011403.1:g.164556T>A | |
| NG_011403.2:g.164556T>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000360256.9:c.6489T>A MANE Select | ENSP00000353393.4:p.Ile2163= | |
| ENST00000644698.1:c.222T>A | ENSP00000495706.1:p.Ile74= | |
| ENST00000330287.10:c.84T>A | ENSP00000327895.6:p.Ile28= | |
| ENST00000360256.8:c.6489T>A | ENSP00000353393.4:p.Ile2163= | |
| NM_000132.3:c.6489T>A | NP_000123.1:p.Ile2163= | |
| NM_019863.2:c.84T>A | NP_063916.1:p.Ile28= | |
| XM_011531126.1:c.6384T>A | XP_011529428.1:p.Ile2128= | |
| NM_000132.4:c.6489T>A MANE Select | NP_000123.1:p.Ile2163= | |
| NM_019863.3:c.84T>A | NP_063916.1:p.Ile28= |