Linked Data
MyVariant Identifiers:
chrX:g.54521581C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.54495148C>G , CM000685.2:g.54495148C>G | GRCh38 |
| NC_000023.10:g.54521581C>G , CM000685.1:g.54521581C>G | GRCh37 |
| NC_000023.9:g.54538306C>G | NCBI36 |
| NG_008054.1:g.6019G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375135.4:c.285G>C MANE Select | ENSP00000364277.3:p.Leu95= | |
| ENST00000375135.3:c.285G>C | ENSP00000364277.3:p.Leu95= | |
| NM_004463.2:c.285G>C | NP_004454.2:p.Leu95= | |
| NM_004463.3:c.285G>C MANE Select | NP_004454.2:p.Leu95= |