Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.50120357A>G , CM000676.2:g.50120357A>G | GRCh38 |
| NC_000014.8:g.50587075A>G , CM000676.1:g.50587075A>G | GRCh37 |
| NC_000014.7:g.49656825A>G | NCBI36 |
| NG_051073.1:g.116337T>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_006939.4:c.3407T>C MANE Select | NP_008870.2:p.Leu1136Ser |
| ENST00000216373.10:c.3407T>C MANE Select | ENSP00000216373.5:p.Leu1136Ser |
| NM_006939.2:c.3407T>C | NP_008870.2:p.Leu1136Ser |
| NM_006939.3:c.3407T>C | NP_008870.2:p.Leu1136Ser |
| ENST00000216373.9:c.3407T>C | ENSP00000216373.5:p.Leu1136Ser |
| ENST00000543680.5:c.3308T>C | ENSP00000445328.1:p.Leu1103Ser |
| XM_005268021.1:c.3227T>C | XP_005268078.1:p.Leu1076Ser |
| XM_011537103.1:c.3368T>C | XP_011535405.1:p.Leu1123Ser |