Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.48966367G= , CM000681.2:g.48966367G= | GRCh38 |
| NC_000019.9:g.49469624G= , CM000681.1:g.49469624G= | GRCh37 |
| NC_000019.8:g.54161436G= | NCBI36 |
| NG_008152.1:g.6059G= | |
| NG_012923.1:g.31987C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000331825.11:c.336G= MANE Select | ENSP00000366525.2:p.Leu112= | |
| ENST00000331825.10:c.336G= | ENSP00000366525.2:p.Leu112= | |
| ENST00000622577.2:c.336G= | ENSP00000484043.1:p.Leu112= | |
| NM_000146.3:c.336G= | NP_000137.2:p.Leu112= | |
| XM_024451447.1:c.846G= | XP_024307215.1:p.Leu282= | |
| NM_000146.4:c.336G= MANE Select | NP_000137.2:p.Leu112= |