Linked Data
MyVariant Identifiers:
chrX:g.150349852T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.151181380T>C , CM000685.2:g.151181380T>C | GRCh38 |
| NC_000023.10:g.150349852T>C , CM000685.1:g.150349852T>C | GRCh37 |
| NC_000023.9:g.150100510T>C | NCBI36 |
| NG_016405.1:g.9797T>C | |
| NG_016405.2:g.9797T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000218316.4:c.1797T>C MANE Select | ENSP00000218316.3:p.Asp599= | |
| ENST00000218316.3:c.1797T>C | ENSP00000218316.3:p.Asp599= | |
| ENST00000617907.1:c.1791T>C | ENSP00000484496.1:p.Asp597= | |
| NM_004224.3:c.1797T>C MANE Select | NP_004215.2:p.Asp599= | |
| XM_011531216.1:c.1056T>C | XP_011529518.1:p.Asp352= | |
| XM_011531216.2:c.1056T>C | XP_011529518.1:p.Asp352= |