Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.169362361G>C , CM000664.2:g.169362361G>C | GRCh38 |
| NC_000002.11:g.170218871G>C , CM000664.1:g.170218871G>C | GRCh37 |
| NC_000002.10:g.169927117G>C | NCBI36 |
| NG_012634.1:g.5252C>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_004525.3:c.39C>G MANE Select | NP_004516.2:p.Leu13= |
| ENST00000649046.1:c.39C>G MANE Select | ENSP00000496870.1:p.Leu13= |
| NM_004525.2:c.39C>G | NP_004516.2:p.Leu13= |
| ENST00000263816.7:c.39C>G | ENSP00000263816.3:p.Leu13= |
| ENST00000443831.1:c.39C>G | ENSP00000409813.1:p.Leu13= |
| XM_011511183.1:c.39C>G | XP_011509485.1:p.Leu13= |
| XM_011511183.3:c.39C>G | XP_011509485.1:p.Leu13= |
| XM_011511185.1:c.39C>G | XP_011509487.1:p.Leu13= |