Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48459754T>C , CM000675.2:g.48459754T>C | GRCh38 |
| NC_000013.10:g.49033890T>C , CM000675.1:g.49033890T>C | GRCh37 |
| NC_000013.9:g.47931891T>C | NCBI36 |
| NG_009009.1:g.161008T>C , LRG_517:g.161008T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000267163.6:c.2027T>C MANE Select | ENSP00000267163.4:p.Leu676Ser | |
| ENST00000643064.1:c.194+78311T>C | ||
| ENST00000650461.1:c.2027T>C | ENSP00000497193.1:p.Leu676Ser | |
| ENST00000267163.4:c.2027T>C | ENSP00000267163.4:p.Leu676Ser | |
| NM_000321.2:c.2027T>C , LRG_517t1:c.2027T>C | NP_000312.2:p.Leu676Ser | |
| XM_011535171.1:c.1766T>C | XP_011533473.1:p.Leu589Ser | |
| XM_011535171.2:c.1766T>C | XP_011533473.1:p.Leu589Ser | |
| NM_000321.3:c.2027T>C MANE Select | NP_000312.2:p.Leu676Ser |