Linked Data
MyVariant Identifiers:
chrX:g.154065962A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154837687A>T , CM000685.2:g.154837687A>T | GRCh38 |
| NC_000023.10:g.154065962A>T , CM000685.1:g.154065962A>T | GRCh37 |
| NC_000023.9:g.153719156A>T | NCBI36 |
| NG_011403.1:g.190037T>A | |
| NG_033065.1:g.1976T>A | |
| NG_011403.2:g.190037T>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000360256.9:c.6966T>A MANE Select | ENSP00000353393.4:p.Thr2322= | |
| ENST00000644698.1:c.699T>A | ENSP00000495706.1:p.Thr233= | |
| ENST00000330287.10:c.561T>A | ENSP00000327895.6:p.Thr187= | |
| ENST00000360256.8:c.6966T>A | ENSP00000353393.4:p.Thr2322= | |
| NM_000132.3:c.6966T>A | NP_000123.1:p.Thr2322= | |
| NM_019863.2:c.561T>A | NP_063916.1:p.Thr187= | |
| XM_011531126.1:c.6861T>A | XP_011529428.1:p.Thr2287= | |
| NM_000132.4:c.6966T>A MANE Select | NP_000123.1:p.Thr2322= | |
| NM_019863.3:c.561T>A | NP_063916.1:p.Thr187= |