Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.137567356T= , CM000685.2:g.137567356T= | GRCh38 |
| NC_000023.10:g.136649515T= , CM000685.1:g.136649515T= | GRCh37 |
| NC_000023.9:g.136477181T= | NCBI36 |
| NG_008115.1:g.6170T= | |
| NG_008115.2:g.6230T= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000287538.10:c.665T= MANE Select | ENSP00000287538.5:p.Met222= | |
| ENST00000287538.9:c.665T= | ENSP00000287538.5:p.Met222= | |
| ENST00000370606.3:c.665T= | ENSP00000359638.3:p.Met222= | |
| NM_003413.3:c.665T= | NP_003404.1:p.Met222= | |
| NM_001330661.1:c.665T= | NP_001317590.1:p.Met222= | |
| NM_003413.4:c.665T= MANE Select | NP_003404.1:p.Met222= |