Linked Data
MyVariant Identifiers:
chr17:g.27822592T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.29495574T>C , CM000679.2:g.29495574T>C | GRCh38 |
| NC_000017.10:g.27822592T>C , CM000679.1:g.27822592T>C | GRCh37 |
| NC_000017.9:g.24846718T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000261716.8:c.846T>C MANE Select | ENSP00000261716.3:p.Leu282= | |
| ENST00000261716.7:c.846T>C | ENSP00000261716.3:p.Leu282= | |
| ENST00000536202.1:c.846T>C | ENSP00000438819.1:p.Leu282= | |
| ENST00000577583.1:n.694T>C | ||
| NM_020791.2:c.846T>C | NP_065842.1:p.Leu282= | |
| NM_025142.1:c.846T>C | NP_079418.1:p.Leu282= | |
| XM_011525060.1:c.846T>C | XP_011523362.1:p.Leu282= | |
| XM_011525060.2:c.846T>C | XP_011523362.1:p.Leu282= | |
| NM_020791.4:c.846T>C MANE Select | NP_065842.1:p.Leu282= |