Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.150297684C>A , CM000667.2:g.150297684C>A | GRCh38 |
| NC_000005.9:g.149677247C>A , CM000667.1:g.149677247C>A | GRCh37 |
| NC_000005.8:g.149657440C>A | NCBI36 |
| NG_051250.1:g.10279G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001012301.4:c.1240G>T MANE Select | NP_001012301.1:p.Ala414Ser |
| ENST00000328668.8:c.1240G>T MANE Select | ENSP00000333395.7:p.Ala414Ser |
| NM_001012301.2:c.1240G>T | NP_001012301.1:p.Ala414Ser |
| NM_001012301.3:c.1240G>T | NP_001012301.1:p.Ala414Ser |
| ENST00000328668.7:c.1240G>T | ENSP00000333395.7:p.Ala414Ser |
| ENST00000515301.2:c.811G>T | ENSP00000426879.2:p.Ala271Ser |