Linked Data
MyVariant Identifiers:
chr22:g.32871031G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.32475044G>A , CM000684.2:g.32475044G>A | GRCh38 |
| NC_000022.10:g.32871031G>A , CM000684.1:g.32871031G>A | GRCh37 |
| NC_000022.9:g.31201031G>A | NCBI36 |
| NG_016001.1:g.5325G>A | |
| NG_016001.2:g.5325G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000266087.12:c.42G>A MANE Select | ENSP00000266087.7:p.Leu14= | |
| ENST00000266087.11:c.42G>A | ENSP00000266087.7:p.Leu14= | |
| ENST00000420700.5:c.42G>A | ENSP00000406155.1:p.Leu14= | |
| ENST00000425028.5:c.42G>A | ENSP00000395823.1:p.Leu14= | |
| ENST00000492535.1:n.30G>A | ||
| NM_012179.3:c.42G>A | NP_036311.3:p.Leu14= | |
| XM_011530106.1:c.-132G>A | XP_011528408.1:n.-132G>A | |
| XM_024452207.1:c.-149G>A | XP_024307975.1:n.-149G>A | |
| NM_012179.4:c.42G>A MANE Select | NP_036311.3:p.Leu14= |