Linked Data
MyVariant Identifiers:
chrX:g.38226586T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.38367333T>G , CM000685.2:g.38367333T>G | GRCh38 |
| NC_000023.10:g.38226586T>G , CM000685.1:g.38226586T>G | GRCh37 |
| NC_000023.9:g.38111530T>G | NCBI36 |
| NG_008471.1:g.19851T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000039007.5:c.120T>G MANE Select | ENSP00000039007.4:p.Arg40= | |
| ENST00000643344.1:c.120T>G | ENSP00000496606.1:p.Arg40= | |
| ENST00000039007.4:c.120T>G | ENSP00000039007.4:p.Arg40= | |
| ENST00000465127.1:c.172-298788T>G | ENSP00000417050.1:n.172-298788T>G | |
| ENST00000488812.1:n.212T>G | ||
| NM_000531.5:c.120T>G | NP_000522.3:p.Arg40= | |
| XM_017029556.1:c.120T>G | XP_016885045.1:p.Arg40= | |
| NM_000531.6:c.120T>G MANE Select | NP_000522.3:p.Arg40= |