Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.15187244T= , CM000681.2:g.15187244T= | GRCh38 |
| NC_000019.9:g.15298055T= , CM000681.1:g.15298055T= | GRCh37 |
| NC_000019.8:g.15159055T= | NCBI36 |
| NG_009819.1:g.18738A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263388.7:c.1701A= MANE Select | ENSP00000263388.1:p.Ser567= | |
| ENST00000263388.6:c.1701A= | ENSP00000263388.1:p.Ser567= | |
| ENST00000601011.1:c.1698A= | ENSP00000473138.1:p.Ser566= | |
| NM_000435.2:c.1701A= | NP_000426.2:p.Ser567= | |
| XM_005259924.3:c.1701A= | XP_005259981.1:p.Ser567= | |
| XM_005259924.4:c.1701A= | XP_005259981.1:p.Ser567= | |
| NM_000435.3:c.1701A= MANE Select | NP_000426.2:p.Ser567= |