Linked Data
MyVariant Identifiers:
chrX:g.29935633C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.29917516C>A , CM000685.2:g.29917516C>A | GRCh38 |
| NC_000023.10:g.29935633C>A , CM000685.1:g.29935633C>A | GRCh37 |
| NC_000023.9:g.29845554C>A | NCBI36 |
| NG_008292.1:g.1334953C>A | |
| NG_008292.2:g.1334953C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378993.6:c.831C>A MANE Select | ENSP00000368278.1:p.Val277= | |
| ENST00000302196.5:c.54C>A | ENSP00000305200.5:p.Val18= | |
| ENST00000378993.5:c.831C>A | ENSP00000368278.1:p.Val277= | |
| NM_014271.3:c.831C>A | NP_055086.1:p.Val277= | |
| XM_005274441.1:c.831C>A | XP_005274498.1:p.Val277= | |
| XM_011545445.1:c.831C>A | XP_011543747.1:p.Val277= | |
| XM_017029240.1:c.831C>A | XP_016884729.1:p.Val277= | |
| XM_017029241.1:c.453C>A | XP_016884730.1:p.Val151= | |
| NM_014271.4:c.831C>A MANE Select | NP_055086.1:p.Val277= |