Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.42843033G>A , CM000670.2:g.42843033G>A | GRCh38 |
| NC_000008.10:g.42698176G>A , CM000670.1:g.42698176G>A | GRCh37 |
| NC_000008.9:g.42817333G>A | NCBI36 |
| NG_011837.1:g.5299C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000254250.7:c.62C>T MANE Select | ENSP00000254250.3:p.Ser21Phe | |
| ENST00000345117.2:c.62C>T | ENSP00000344966.2:p.Ser21Phe | |
| ENST00000529779.1:c.62C>T | ENSP00000433912.1:p.Ser21Phe | |
| NM_018105.2:c.62C>T | NP_060575.1:p.Ser21Phe | |
| NM_199003.1:c.62C>T | NP_945354.1:p.Ser21Phe | |
| NM_018105.3:c.62C>T MANE Select | NP_060575.1:p.Ser21Phe | |
| NM_199003.2:c.62C>T | NP_945354.1:p.Ser21Phe |