Linked Data
MyVariant Identifiers:
chrX:g.54492171T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.54465738T>G , CM000685.2:g.54465738T>G | GRCh38 |
| NC_000023.10:g.54492171T>G , CM000685.1:g.54492171T>G | GRCh37 |
| NC_000023.9:g.54508896T>G | NCBI36 |
| NG_008054.1:g.35429A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375135.4:c.1455A>C MANE Select | ENSP00000364277.3:p.Thr485= | |
| ENST00000375135.3:c.1455A>C | ENSP00000364277.3:p.Thr485= | |
| NM_004463.2:c.1455A>C | NP_004454.2:p.Thr485= | |
| NM_004463.3:c.1455A>C MANE Select | NP_004454.2:p.Thr485= |