Linked Data
MyVariant Identifiers:
chr16:g.57017302C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.56983390C>T , CM000678.2:g.56983390C>T | GRCh38 |
| NC_000016.9:g.57017302C>T , CM000678.1:g.57017302C>T | GRCh37 |
| NC_000016.8:g.55574803C>T | NCBI36 |
| NG_008952.1:g.26468C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000200676.8:c.1386C>T MANE Select | ENSP00000200676.3:p.Asn462= | |
| ENST00000650358.1:n.1784C>T | ||
| ENST00000200676.7:c.1386C>T | ENSP00000200676.3:p.Asn462= | |
| ENST00000379780.6:c.1206C>T | ENSP00000369106.2:p.Asn402= | |
| ENST00000566128.1:c.1191C>T | ENSP00000456276.1:p.Asn397= | |
| NM_000078.2:c.1386C>T | NP_000069.2:p.Asn462= | |
| NM_001286085.1:c.1206C>T | NP_001273014.1:p.Asn402= | |
| NM_000078.3:c.1386C>T MANE Select | NP_000069.2:p.Asn462= | |
| NM_001286085.2:c.1206C>T | NP_001273014.1:p.Asn402= |