Linked Data
MyVariant Identifiers:
chrX:g.30326434G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.30308317G>C , CM000685.2:g.30308317G>C | GRCh38 |
| NC_000023.10:g.30326434G>C , CM000685.1:g.30326434G>C | GRCh37 |
| NC_000023.9:g.30236355G>C | NCBI36 |
| NG_009814.1:g.6062C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378970.5:c.1047C>G MANE Select | ENSP00000368253.4:p.Ala349= | |
| ENST00000378963.1:c.162C>G | ENSP00000368246.1:p.Ala54= | |
| ENST00000378970.4:c.1047C>G | ENSP00000368253.4:p.Ala349= | |
| NM_000475.4:c.1047C>G | NP_000466.2:p.Ala349= | |
| NM_000475.5:c.1047C>G MANE Select | NP_000466.2:p.Ala349= |