Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.117835522A>G , CM000670.2:g.117835522A>G | GRCh38 |
| NC_000008.10:g.118847761A>G , CM000670.1:g.118847761A>G | GRCh37 |
| NC_000008.9:g.118916942A>G | NCBI36 |
| NG_007455.2:g.281298T>C , LRG_493:g.281298T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684189.1:n.553T>C | ||
| ENST00000378204.7:c.1086T>C MANE Select | ENSP00000367446.3:p.Asn362= | |
| ENST00000436216.2:c.454T>C | ||
| ENST00000378204.6:c.1086T>C | ENSP00000367446.2:p.Asn362= | |
| ENST00000436216.1:c.454T>C | ||
| ENST00000437196.1:c.103T>C | ENSP00000407299.1:p.Trp35Arg | |
| NM_000127.2:c.1086T>C , LRG_493t1:c.1086T>C | NP_000118.2:p.Asn362= | |
| NM_000127.3:c.1086T>C MANE Select | NP_000118.2:p.Asn362= |