Linked Data
MyVariant Identifiers:
chr22:g.28146912G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.27750924G>T , CM000684.2:g.27750924G>T | GRCh38 |
| NC_000022.10:g.28146912G>T , CM000684.1:g.28146912G>T | GRCh37 |
| NC_000022.9:g.26476912G>T | NCBI36 |
| NG_023258.1:g.55575C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000703102.1:n.479C>A | ||
| ENST00000302326.5:c.3954C>A MANE Select | ENSP00000304956.4:p.Ala1318= | |
| ENST00000302326.4:c.3954C>A | ENSP00000304956.4:p.Ala1318= | |
| ENST00000424656.1:c.307C>A | ||
| ENST00000497225.1:n.310C>A | ||
| NM_002430.2:c.3954C>A | NP_002421.3:p.Ala1318= | |
| NM_002430.3:c.3954C>A MANE Select | NP_002421.3:p.Ala1318= |