Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.23680746T= , CM000685.2:g.23680746T= | GRCh38 |
| NC_000023.10:g.23698863T= , CM000685.1:g.23698863T= | GRCh37 |
| NC_000023.9:g.23608784T= | NCBI36 |
| NG_012563.1:g.18219T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_006406.2:c.599+1459T= MANE Select | NP_006397.1:n.599+1459T= |
| ENST00000379341.9:c.599+1459T= MANE Select | ENSP00000368646.4:n.599+1459T= |
| NM_006406.1:c.599+1459T= | NP_006397.1:n.599+1459T= |
| ENST00000379341.8:c.599+1459T= | ENSP00000368646.4:n.599+1459T= |
| ENST00000439422.1:c.231+1459T= | |
| XM_005274438.1:c.557+1459T= | XP_005274495.1:n.557+1459T= |