Linked Data
MyVariant Identifiers:
chr16:g.57017251G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.56983339G>T , CM000678.2:g.56983339G>T | GRCh38 |
| NC_000016.9:g.57017251G>T , CM000678.1:g.57017251G>T | GRCh37 |
| NC_000016.8:g.55574752G>T | NCBI36 |
| NG_008952.1:g.26417G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000200676.8:c.1335G>T MANE Select | ENSP00000200676.3:p.Val445= | |
| ENST00000650358.1:n.1733G>T | ||
| ENST00000200676.7:c.1335G>T | ENSP00000200676.3:p.Val445= | |
| ENST00000379780.6:c.1155G>T | ENSP00000369106.2:p.Val385= | |
| ENST00000566128.1:c.1140G>T | ENSP00000456276.1:p.Val380= | |
| NM_000078.2:c.1335G>T | NP_000069.2:p.Val445= | |
| NM_001286085.1:c.1155G>T | NP_001273014.1:p.Val385= | |
| NM_000078.3:c.1335G>T MANE Select | NP_000069.2:p.Val445= | |
| NM_001286085.2:c.1155G>T | NP_001273014.1:p.Val385= |