Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.19116981T= , CM000669.2:g.19116981T= | GRCh38 |
| NC_000007.13:g.19156604T= , CM000669.1:g.19156604T= | GRCh37 |
| NC_000007.12:g.19123129T= | NCBI36 |
| NG_008114.1:g.5692A= | |
| NG_008114.2:g.5692A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000242261.6:c.341A= MANE Select | ENSP00000242261.5:p.Asn114= | |
| ENST00000242261.5:c.341A= | ENSP00000242261.5:p.Asn114= | |
| ENST00000354571.5:c.138A= | ||
| NM_000474.3:c.341A= | NP_000465.1:p.Asn114= | |
| XM_011515496.1:c.341A= | XP_011513798.1:p.Asn114= | |
| NR_149001.1:n.692A= | ||
| NM_000474.4:c.341A= MANE Select | NP_000465.1:p.Asn114= | |
| NR_149001.2:n.656A= |