MyVariant.info:
GRCh37
chr16:g.14041799T>C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.13947942T>C , CM000678.2:g.13947942T>C | GRCh38 |
| NC_000016.9:g.14041799T>C , CM000678.1:g.14041799T>C | GRCh37 |
| NC_000016.8:g.13949300T>C | NCBI36 |
| NG_011442.1:g.32786T>C , LRG_463:g.32786T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682617.1:c.2484T>C | ENSP00000507912.1:p.Asn828= | |
| ENST00000683962.1:c.*2040T>C | ENSP00000506854.1:n.*2040T>C | |
| ENST00000311895.8:c.2346T>C MANE Select | ENSP00000310520.7:p.Asn782= | |
| ENST00000311895.7:c.2346T>C | ENSP00000310520.7:p.Asn782= | |
| ENST00000389138.7:n.1623T>C | ||
| ENST00000462862.1:c.659T>C | ENSP00000461322.1:n.659T>C | |
| NM_005236.2:c.2346T>C , LRG_463t1:c.2346T>C | NP_005227.1:p.Asn782= | |
| XM_011522424.1:c.2484T>C | XP_011520726.1:p.Asn828= | |
| XM_011522425.1:c.1803T>C | XP_011520727.1:p.Asn601= | |
| XM_011522426.1:c.1557T>C | XP_011520728.1:p.Asn519= | |
| XM_011522427.1:c.996T>C | XP_011520729.1:p.Asn332= | |
| XR_932805.1:n.2505T>C | ||
| XM_011522424.3:c.2484T>C | XP_011520726.1:p.Asn828= | |
| XM_017023043.2:c.1557T>C | XP_016878532.1:p.Asn519= | |
| NM_005236.3:c.2346T>C MANE Select | NP_005227.1:p.Asn782= |