Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.3857792A= , CM000682.2:g.3857792A= | GRCh38 |
| NC_000020.10:g.3838439A= , CM000682.1:g.3838439A= | GRCh37 |
| NC_000020.9:g.3786439A= | NCBI36 |
| NG_030028.1:g.15994A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000428216.4:c.275A= MANE Select | ENSP00000401980.2:p.Tyr92= | |
| ENST00000416600.6:c.-132+3051A= | ENSP00000413749.2:n.-132+3051A= | |
| ENST00000428216.3:c.275A= | ENSP00000401980.2:p.Tyr92= | |
| NM_001206491.1:c.-132+3051A= | NP_001193420.1:n.-132+3051A= | |
| NM_020746.4:c.275A= | NP_065797.2:p.Tyr92= | |
| NR_037921.1:n.447A= | ||
| NM_020746.5:c.275A= MANE Select | NP_065797.2:p.Tyr92= | |
| NR_037921.2:n.412A= | ||
| NM_001206491.2:c.-132+3051A= | NP_001193420.1:n.-132+3051A= | |
| NM_001385663.1:c.-273A= | NP_001372592.1:n.-273A= |