Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.65239782A= , CM000674.2:g.65239782A= | GRCh38 |
| NC_000012.11:g.65633562A= , CM000674.1:g.65633562A= | GRCh37 |
| NC_000012.10:g.63919829A= | NCBI36 |
| NG_016210.1:g.75212A= | |
| NG_016210.2:g.75212A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000308330.3:c.1922-147A= MANE Select | ENSP00000308369.2:n.1922-147A= | |
| ENST00000308330.2:c.1922-147A= | ENSP00000308369.2:n.1922-147A= | |
| NM_001167614.1:c.1919-147A= | NP_001161086.1:n.1919-147A= | |
| NM_014319.4:c.1922-147A= | NP_055134.2:n.1922-147A= | |
| NM_014319.5:c.1922-147A= MANE Select | NP_055134.2:n.1922-147A= | |
| NM_001167614.2:c.1919-147A= | NP_001161086.1:n.1919-147A= |