Linked Data
dbSNP Id:
rs2085657338
gnomAD v3:
15-43600583-T-G
gnomAD v4:
15-43600583-T-G
MyVariant Identifiers:
chr15:g.43892781T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.43600583T>G , CM000677.2:g.43600583T>G | GRCh38 |
| NC_000015.9:g.43892781T>G , CM000677.1:g.43892781T>G | GRCh37 |
| NC_000015.8:g.41680073T>G | NCBI36 |
| NG_011636.1:g.23218A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000450892.7:c.4944A>C (STRC) MANE Select | ENSP00000401513.2:p.Pro1648= | |
| ENST00000411560.1:n.142+1050T>G (CKMT1B) | ||
| ENST00000428650.5:c.*1977A>C (STRC) | ENSP00000415991.1:n.*1977A>C | |
| ENST00000440125.5:c.*2736A>C (STRC) | ENSP00000394866.1:n.*2736A>C | |
| ENST00000448437.6:n.2064A>C (STRC) | ||
| ENST00000450892.6:c.4944A>C (STRC) | ENSP00000401513.2:p.Pro1648= | |
| ENST00000460952.1:n.523A>C (STRC) | ||
| ENST00000471703.5:n.2898A>C (STRC) | ||
| ENST00000485556.5:n.3799A>C (STRC) | ||
| ENST00000541030.5:c.2625A>C (STRC) | ENSP00000440413.1:p.Pro875= | |
| NM_153700.2:c.4944A>C (STRC) MANE Select | NP_714544.1:p.Pro1648= | |
| XM_011521277.1:c.5433A>C (STRC) | XP_011519579.1:p.Pro1811= | |
| XM_011521278.1:c.5049A>C (STRC) | XP_011519580.1:p.Pro1683= | |
| XM_011521279.1:c.5049A>C (STRC) | XP_011519581.1:p.Pro1683= |