Linked Data
MyVariant Identifiers:
chrX:g.152955903G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.153690448G>C , CM000685.2:g.153690448G>C | GRCh38 |
| NC_000023.10:g.152955903G>C , CM000685.1:g.152955903G>C | GRCh37 |
| NC_000023.9:g.152609097G>C | NCBI36 |
| NG_012016.1:g.7152G>C | |
| NG_012016.2:g.7152G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000253122.10:c.336G>C MANE Select | ENSP00000253122.5:p.Leu112= | |
| ENST00000675713.1:n.90G>C | ||
| ENST00000253122.9:c.336G>C | ENSP00000253122.5:p.Leu112= | |
| ENST00000430077.6:c.-10G>C | ENSP00000403041.2:n.-10G>C | |
| ENST00000476466.1:n.188G>C | ||
| NM_001142805.1:c.336G>C | NP_001136277.1:p.Leu112= | |
| NM_001142806.1:c.-10G>C | NP_001136278.1:n.-10G>C | |
| NM_005629.3:c.336G>C | NP_005620.1:p.Leu112= | |
| NM_005629.4:c.336G>C MANE Select | NP_005620.1:p.Leu112= | |
| NM_001142805.2:c.336G>C | NP_001136277.1:p.Leu112= |