Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.202556560T= , CM000664.2:g.202556560T= | GRCh38 |
| NC_000002.11:g.203421283T= , CM000664.1:g.203421283T= | GRCh37 |
| NC_000002.10:g.203129528T= | NCBI36 |
| NG_009363.1:g.185234T= , LRG_712:g.185234T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374580.10:c.2866+29T= MANE Select | ENSP00000363708.4:n.2866+29T= | |
| ENST00000638587.1:c.2797+29T= | ENSP00000491062.1:n.2797+29T= | |
| ENST00000374574.2:c.1587-3136T= | ENSP00000363702.2:n.1587-3136T= | |
| ENST00000374580.8:c.2866+29T= | ENSP00000363708.4:n.2866+29T= | |
| NM_001204.6:c.2866+29T= , LRG_712t1:c.2866+29T= | NP_001195.2:n.2866+29T= | |
| XM_011511687.1:c.2866+29T= | XP_011509989.1:n.2866+29T= | |
| XM_011511688.1:c.1587-3136T= | XP_011509990.1:n.1587-3136T= | |
| NM_001204.7:c.2866+29T= MANE Select | NP_001195.2:n.2866+29T= |