MyVariant.info:
GRCh37
chrX:g.138643816C>G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.139561657C>G , CM000685.2:g.139561657C>G | GRCh38 |
| NC_000023.10:g.138643816C>G , CM000685.1:g.138643816C>G | GRCh37 |
| NC_000023.9:g.138471482C>G | NCBI36 |
| NG_007994.1:g.35922C>G , LRG_556:g.35922C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000218099.7:c.972C>G MANE Select | ENSP00000218099.2:p.Pro324= | |
| ENST00000643157.1:n.1639C>G | ||
| ENST00000218099.6:c.972C>G | ENSP00000218099.2:p.Pro324= | |
| ENST00000394090.2:c.858C>G | ENSP00000377650.2:p.Pro286= | |
| NM_000133.3:c.972C>G , LRG_556t1:c.972C>G | NP_000124.1:p.Pro324= | |
| NM_001313913.1:c.858C>G | NP_001300842.1:p.Pro286= | |
| XM_005262397.3:c.843C>G | XP_005262454.1:p.Pro281= | |
| XM_005262397.4:c.843C>G | XP_005262454.1:p.Pro281= | |
| NM_000133.4:c.972C>G MANE Select | NP_000124.1:p.Pro324= | |
| NM_001313913.2:c.858C>G | NP_001300842.1:p.Pro286= |