Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48456204G>C , CM000675.2:g.48456204G>C | GRCh38 |
| NC_000013.10:g.49030340G>C , CM000675.1:g.49030340G>C | GRCh37 |
| NC_000013.9:g.47928341G>C | NCBI36 |
| NG_009009.1:g.157458G>C , LRG_517:g.157458G>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000321.3:c.1815G>C MANE Select | NP_000312.2:p.Met605Ile |
| ENST00000267163.6:c.1815G>C MANE Select | ENSP00000267163.4:p.Met605Ile |
| NM_000321.2:c.1815G>C , LRG_517t1:c.1815G>C | NP_000312.2:p.Met605Ile |
| ENST00000267163.4:c.1815G>C | ENSP00000267163.4:p.Met605Ile |
| ENST00000480491.1:n.514G>C | |
| ENST00000643064.1:c.194+74761G>C | |
| ENST00000650461.1:c.1815G>C | ENSP00000497193.1:p.Met605Ile |
| XM_011535171.1:c.1554G>C | XP_011533473.1:p.Met518Ile |
| XM_011535171.2:c.1554G>C | XP_011533473.1:p.Met518Ile |