Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.159322749A= , CM000667.2:g.159322749A= | GRCh38 |
| NC_000005.9:g.158749757A= , CM000667.1:g.158749757A= | GRCh37 |
| NC_000005.8:g.158682335A= | NCBI36 |
| NG_009618.1:g.12725T= , LRG_71:g.12725T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696750.1:c.-148-2229T= | ENSP00000512849.1:n.-148-2229T= | |
| ENST00000696751.1:c.364+305T= | ENSP00000512850.1:n.364+305T= | |
| ENST00000231228.3:c.365-238T= MANE Select | ENSP00000231228.2:n.365-238T= | |
| ENST00000231228.2:c.365-238T= | ENSP00000231228.2:n.365-238T= | |
| NM_002187.2:c.365-238T= , LRG_71t1:c.365-238T= | NP_002178.2:n.365-238T= | |
| XR_001742945.1:n.147+2153A= | ||
| NM_002187.3:c.365-238T= MANE Select | NP_002178.2:n.365-238T= |