Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.19965319G>C , CM000670.2:g.19965319G>C | GRCh38 |
| NC_000008.10:g.19822830G>C , CM000670.1:g.19822830G>C | GRCh37 |
| NC_000008.9:g.19867110G>C | NCBI36 |
| NG_008855.1:g.31249G>C | |
| NG_008855.2:g.68603G>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000237.3:c.*9G>C MANE Select | NP_000228.1:n.*9G>C |
| ENST00000650287.1:c.*9G>C MANE Select | ENSP00000497642.1:n.*9G>C |
| NM_000237.2:c.*9G>C | NP_000228.1:n.*9G>C |
| ENST00000311322.8:c.*9G>C | ENSP00000309757.6:n.*9G>C |
| ENST00000650478.1:c.377G>C | ENSP00000497560.1:n.377G>C |