Linked Data
MyVariant Identifiers:
chrX:g.30322783A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.30304666A>G , CM000685.2:g.30304666A>G | GRCh38 |
| NC_000023.10:g.30322783A>G , CM000685.1:g.30322783A>G | GRCh37 |
| NC_000023.9:g.30232704A>G | NCBI36 |
| NG_009814.1:g.9713T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378970.5:c.1326T>C MANE Select | ENSP00000368253.4:p.Asn442= | |
| ENST00000378970.4:c.1326T>C | ENSP00000368253.4:p.Asn442= | |
| NM_000475.4:c.1326T>C | NP_000466.2:p.Asn442= | |
| NM_000475.5:c.1326T>C MANE Select | NP_000466.2:p.Asn442= |