Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.48965843A= , CM000681.2:g.48965843A= | GRCh38 |
| NC_000019.9:g.49469100A= , CM000681.1:g.49469100A= | GRCh37 |
| NC_000019.8:g.54160912A= | NCBI36 |
| NG_008152.1:g.5535A= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000331825.11:c.176A= MANE Select | ENSP00000366525.2:p.Lys59= | |
| ENST00000331825.10:c.176A= | ENSP00000366525.2:p.Lys59= | |
| ENST00000622577.2:c.176A= | ENSP00000484043.1:p.Lys59= | |
| NM_000146.3:c.176A= | NP_000137.2:p.Lys59= | |
| XM_024451447.1:c.686A= | XP_024307215.1:p.Lys229= | |
| NM_000146.4:c.176A= MANE Select | NP_000137.2:p.Lys59= |