Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48364892A>C , CM000675.2:g.48364892A>C | GRCh38 |
| NC_000013.10:g.48939028A>C , CM000675.1:g.48939028A>C | GRCh37 |
| NC_000013.9:g.47837029A>C | NCBI36 |
| NG_009009.1:g.66146A>C , LRG_517:g.66146A>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000321.3:c.862-2A>C MANE Select | NP_000312.2:n.862-2A>C |
| ENST00000267163.6:c.862-2A>C MANE Select | ENSP00000267163.4:n.862-2A>C |
| NM_000321.2:c.862-2A>C , LRG_517t1:c.862-2A>C | NP_000312.2:n.862-2A>C |
| ENST00000267163.4:c.862-2A>C | ENSP00000267163.4:n.862-2A>C |
| ENST00000650461.1:c.862-2A>C | ENSP00000497193.1:n.862-2A>C |
| XM_011535171.1:c.601-2A>C | XP_011533473.1:n.601-2A>C |
| XM_011535171.2:c.601-2A>C | XP_011533473.1:n.601-2A>C |