MyVariant.info:
GRCh37
chr16:g.16110385T>G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.16016528T>G , CM000678.2:g.16016528T>G | GRCh38 |
| NC_000016.9:g.16110385T>G , CM000678.1:g.16110385T>G | GRCh37 |
| NC_000016.8:g.16017886T>G | NCBI36 |
| NG_028268.1:g.71952T>G | |
| NG_028268.2:g.71952T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000399408.7:c.522T>G | ENSP00000382340.4:p.Thr174= | |
| ENST00000399410.8:c.522T>G MANE Select | ENSP00000382342.3:p.Thr174= | |
| ENST00000572882.3:c.522T>G | ENSP00000461615.2:p.Thr174= | |
| ENST00000574224.2:n.597T>G | ||
| ENST00000677164.1:c.489+1900T>G | ENSP00000502873.1:n.489+1900T>G | |
| ENST00000678422.1:c.522T>G | ENSP00000503954.1:p.Thr174= | |
| ENST00000679043.1:n.474T>G | ||
| ENST00000399408.6:c.-457T>G | ENSP00000382340.3:n.-457T>G | |
| ENST00000399410.7:c.522T>G | ENSP00000382342.3:p.Thr174= | |
| ENST00000572882.2:c.217T>G | ||
| ENST00000574224.1:n.122T>G | ||
| NM_004996.3:c.522T>G | NP_004987.2:p.Thr174= | |
| XM_011522497.1:c.498T>G | XP_011520799.1:p.Thr166= | |
| XM_011522498.1:c.576T>G | XP_011520800.1:p.Thr192= | |
| XM_011522498.2:c.576T>G | XP_011520800.1:p.Thr192= | |
| XM_017023237.1:c.576T>G | XP_016878726.1:p.Thr192= | |
| XM_017023238.1:c.543+1900T>G | XP_016878727.1:n.543+1900T>G | |
| XM_017023239.1:c.438T>G | XP_016878728.1:p.Thr146= | |
| XM_017023240.1:c.576T>G | XP_016878729.1:p.Thr192= | |
| XM_017023241.1:c.405+6627T>G | XP_016878730.1:n.405+6627T>G | |
| XM_017023242.1:c.576T>G | XP_016878731.1:p.Thr192= | |
| XM_017023243.2:c.576T>G | XP_016878732.1:p.Thr192= | |
| NM_004996.4:c.522T>G MANE Select | NP_004987.2:p.Thr174= |