Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48456276G>T , CM000675.2:g.48456276G>T | GRCh38 |
| NC_000013.10:g.49030412G>T , CM000675.1:g.49030412G>T | GRCh37 |
| NC_000013.9:g.47928413G>T | NCBI36 |
| NG_009009.1:g.157530G>T , LRG_517:g.157530G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000321.3:c.1887G>T MANE Select | NP_000312.2:p.Glu629Asp |
| ENST00000267163.6:c.1887G>T MANE Select | ENSP00000267163.4:p.Glu629Asp |
| NM_000321.2:c.1887G>T , LRG_517t1:c.1887G>T | NP_000312.2:p.Glu629Asp |
| ENST00000267163.4:c.1887G>T | ENSP00000267163.4:p.Glu629Asp |
| ENST00000480491.1:n.586G>T | |
| ENST00000643064.1:c.194+74833G>T | |
| ENST00000650461.1:c.1887G>T | ENSP00000497193.1:p.Glu629Asp |
| XM_011535171.1:c.1626G>T | XP_011533473.1:p.Glu542Asp |
| XM_011535171.2:c.1626G>T | XP_011533473.1:p.Glu542Asp |