Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48381245A>C , CM000675.2:g.48381245A>C | GRCh38 |
| NC_000013.10:g.48955381A>C , CM000675.1:g.48955381A>C | GRCh37 |
| NC_000013.9:g.47853382A>C | NCBI36 |
| NG_009009.1:g.82499A>C , LRG_517:g.82499A>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000321.3:c.1499-2A>C MANE Select | NP_000312.2:n.1499-2A>C |
| ENST00000267163.6:c.1499-2A>C MANE Select | ENSP00000267163.4:n.1499-2A>C |
| NM_000321.2:c.1499-2A>C , LRG_517t1:c.1499-2A>C | NP_000312.2:n.1499-2A>C |
| ENST00000267163.4:c.1499-2A>C | ENSP00000267163.4:n.1499-2A>C |
| ENST00000650461.1:c.1499-2A>C | ENSP00000497193.1:n.1499-2A>C |
| XM_011535171.1:c.1238-2A>C | XP_011533473.1:n.1238-2A>C |
| XM_011535171.2:c.1238-2A>C | XP_011533473.1:n.1238-2A>C |