Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.39507258G>C , CM000681.2:g.39507258G>C | GRCh38 |
| NC_000019.9:g.39997898G>C , CM000681.1:g.39997898G>C | GRCh37 |
| NC_000019.8:g.44689738G>C | NCBI36 |
| NG_008256.1:g.13342G>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_203486.3:c.1313G>C MANE Select | NP_982353.1:p.Cys438Ser |
| ENST00000356433.10:c.1313G>C MANE Select | ENSP00000348810.4:p.Cys438Ser |
| NM_016941.3:c.1313G>C | NP_058637.1:p.Cys438Ser |
| NM_016941.4:c.1313G>C | NP_058637.1:p.Cys438Ser |
| NM_203486.2:c.1313G>C | NP_982353.1:p.Cys438Ser |
| ENST00000205143.4:c.1313G>C | ENSP00000205143.3:p.Cys438Ser |
| ENST00000356433.9:c.1313G>C | ENSP00000348810.4:p.Cys438Ser |
| ENST00000596614.5:c.629G>C | ENSP00000471688.1:p.Cys210Ser |