Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154896229C= , CM000685.2:g.154896229C= | GRCh38 |
| NC_000023.10:g.154124504C= , CM000685.1:g.154124504C= | GRCh37 |
| NC_000023.9:g.153777698C= | NCBI36 |
| NG_011403.1:g.131495G= | |
| NG_011403.2:g.131495G= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000360256.9:c.6277G= MANE Select | ENSP00000353393.4:p.Asp2093= | |
| ENST00000360256.8:c.6277G= | ENSP00000353393.4:p.Asp2093= | |
| NM_000132.3:c.6277G= | NP_000123.1:p.Asp2093= | |
| XM_011531126.1:c.6172G= | XP_011529428.1:p.Asp2058= | |
| NM_000132.4:c.6277G= MANE Select | NP_000123.1:p.Asp2093= |