Linked Data
MyVariant Identifiers:
chrX:g.8699916C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.8731875C>G , CM000685.2:g.8731875C>G | GRCh38 |
| NC_000023.10:g.8699916C>G , CM000685.1:g.8699916C>G | GRCh37 |
| NC_000023.9:g.8659916C>G | NCBI36 |
| NG_007088.1:g.5312G>C | |
| NG_007088.2:g.5312G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262648.8:c.162G>C MANE Select | ENSP00000262648.3:p.Leu54= | |
| ENST00000262648.7:c.162G>C | ENSP00000262648.3:p.Leu54= | |
| ENST00000619786.1:c.159G>C | ENSP00000478734.1:p.Leu53= | |
| NM_000216.2:c.162G>C | NP_000207.2:p.Leu54= | |
| XM_005274501.3:c.162G>C | XP_005274558.1:p.Leu54= | |
| NM_000216.3:c.162G>C | NP_000207.2:p.Leu54= | |
| XM_005274501.4:c.162G>C | XP_005274558.1:p.Leu54= | |
| NM_000216.4:c.162G>C MANE Select | NP_000207.2:p.Leu54= |