MyVariant.info:
GRCh37
chr16:g.4033436T>G
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.3983435T>G , CM000678.2:g.3983435T>G | GRCh38 |
| NC_000016.9:g.4033436T>G , CM000678.1:g.4033436T>G | GRCh37 |
| NC_000016.8:g.3973437T>G | NCBI36 |
| NG_011434.1:g.137751A>C | |
| NG_011434.2:g.137751A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000294016.8:c.2316A>C MANE Select | ENSP00000294016.3:p.Ile772= | |
| ENST00000294016.7:c.2316A>C | ENSP00000294016.3:p.Ile772= | |
| ENST00000574721.1:n.716A>C | ||
| ENST00000575550.5:n.526A>C | ||
| ENST00000576936.5:c.13A>C | ||
| NM_001116.3:c.2316A>C | NP_001107.2:p.Ile772= | |
| XM_005255079.2:c.2373A>C | XP_005255136.1:p.Ile791= | |
| XM_011522353.1:c.2373A>C | XP_011520655.1:p.Ile791= | |
| XM_005255079.3:c.2373A>C | XP_005255136.1:p.Ile791= | |
| XM_011522353.2:c.2373A>C | XP_011520655.1:p.Ile791= | |
| NM_001116.4:c.2316A>C MANE Select | NP_001107.2:p.Ile772= |