Linked Data
dbSNP Id:
rs5910
gnomAD v4:
17-44372421-G-T
MyVariant Identifiers:
chr17:g.42449789G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.44372421G>T , CM000679.2:g.44372421G>T | GRCh38 |
| NC_000017.10:g.42449789G>T , CM000679.1:g.42449789G>T | GRCh37 |
| NC_000017.9:g.39805315G>T | NCBI36 |
| NG_008331.1:g.22085C>A , LRG_479:g.22085C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262407.6:c.3063C>A MANE Select | ENSP00000262407.5:p.Val1021= | |
| ENST00000648408.1:c.2377C>A | ||
| ENST00000262407.5:c.3063C>A | ENSP00000262407.5:p.Val1021= | |
| ENST00000587295.5:c.256C>A | ||
| ENST00000588098.1:c.40C>A | ||
| NM_000419.3:c.3063C>A , LRG_479t1:c.3063C>A | NP_000410.2:p.Val1021= | |
| XM_011524749.1:c.2961C>A | XP_011523051.1:p.Val987= | |
| XM_011524750.1:c.2946C>A | XP_011523052.1:p.Val982= | |
| NM_000419.4:c.3063C>A | NP_000410.2:p.Val1021= | |
| NM_000419.5:c.3063C>A MANE Select | NP_000410.2:p.Val1021= |