MyVariant.info:
GRCh37
chrX:g.154091401A>T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154863126A>T , CM000685.2:g.154863126A>T | GRCh38 |
| NC_000023.10:g.154091401A>T , CM000685.1:g.154091401A>T | GRCh37 |
| NC_000023.9:g.153744595A>T | NCBI36 |
| NG_011403.1:g.164598T>A | |
| NG_011403.2:g.164598T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360256.9:c.6531T>A MANE Select | ENSP00000353393.4:p.Ile2177= | |
| ENST00000644698.1:c.264T>A | ENSP00000495706.1:p.Ile88= | |
| ENST00000330287.10:c.126T>A | ENSP00000327895.6:p.Ile42= | |
| ENST00000360256.8:c.6531T>A | ENSP00000353393.4:p.Ile2177= | |
| NM_000132.3:c.6531T>A | NP_000123.1:p.Ile2177= | |
| NM_019863.2:c.126T>A | NP_063916.1:p.Ile42= | |
| XM_011531126.1:c.6426T>A | XP_011529428.1:p.Ile2142= | |
| NM_000132.4:c.6531T>A MANE Select | NP_000123.1:p.Ile2177= | |
| NM_019863.3:c.126T>A | NP_063916.1:p.Ile42= |