Linked Data
MyVariant Identifiers:
chr12:g.58157956C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.57764173C>G , CM000674.2:g.57764173C>G | GRCh38 |
| NC_000012.11:g.58157956C>G , CM000674.1:g.58157956C>G | GRCh37 |
| NC_000012.10:g.56444223C>G | NCBI36 |
| NG_007076.1:g.8021G>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000713544.1:c.1221G>C | ENSP00000518840.1:p.Leu407= | |
| ENST00000713545.1:c.*145G>C | ENSP00000518841.1:n.*145G>C | |
| ENST00000228606.9:c.1140G>C MANE Select | ENSP00000228606.4:p.Leu380= | |
| ENST00000228606.8:c.1140G>C | ENSP00000228606.4:p.Leu380= | |
| ENST00000546567.5:c.435G>C | ENSP00000449472.1:p.Leu145= | |
| ENST00000547344.5:n.1279G>C | ||
| NM_000785.3:c.1140G>C | NP_000776.1:p.Leu380= | |
| NM_000785.4:c.1140G>C MANE Select | NP_000776.1:p.Leu380= |