Linked Data
MyVariant Identifiers:
chrX:g.154194257T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154965982T>G , CM000685.2:g.154965982T>G | GRCh38 |
| NC_000023.10:g.154194257T>G , CM000685.1:g.154194257T>G | GRCh37 |
| NC_000023.9:g.153847451T>G | NCBI36 |
| NG_011403.1:g.61742A>C | |
| NG_011403.2:g.61742A>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000360256.9:c.1431A>C MANE Select | ENSP00000353393.4:p.Gly477= | |
| ENST00000647125.1:c.*1307A>C | ENSP00000496062.1:n.*1307A>C | |
| ENST00000360256.8:c.1431A>C | ENSP00000353393.4:p.Gly477= | |
| ENST00000483822.2:n.251A>C | ||
| NM_000132.3:c.1431A>C | NP_000123.1:p.Gly477= | |
| XM_011531126.1:c.1326A>C | XP_011529428.1:p.Gly442= | |
| NM_000132.4:c.1431A>C MANE Select | NP_000123.1:p.Gly477= |