Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.855808G>T , CM000681.2:g.855808G>T | GRCh38 |
| NC_000019.9:g.855808G>T , CM000681.1:g.855808G>T | GRCh37 |
| NC_000019.8:g.806808G>T | NCBI36 |
| NG_007274.1:g.1144G>T , LRG_46:g.1144G>T | |
| NG_009627.1:g.8518G>T , LRG_57:g.8518G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263621.2:c.597+14G>T MANE Select | ENSP00000263621.1:n.597+14G>T | |
| ENST00000263621.1:c.597+14G>T | ENSP00000263621.1:n.597+14G>T | |
| ENST00000590230.5:c.597+14G>T | ENSP00000466090.1:n.597+14G>T | |
| NM_001972.2:c.597+14G>T , LRG_57t1:c.597+14G>T | NP_001963.1:n.597+14G>T | |
| XM_011527775.1:c.597+14G>T | XP_011526077.1:n.597+14G>T | |
| XM_011527776.1:c.597+14G>T | XP_011526078.1:n.597+14G>T | |
| NM_001972.3:c.597+14G>T | NP_001963.1:n.597+14G>T | |
| NM_001972.4:c.597+14G>T MANE Select | NP_001963.1:n.597+14G>T |