Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.170108247G= , CM000667.2:g.170108247G= | GRCh38 |
| NC_000005.9:g.169535251G= , CM000667.1:g.169535251G= | GRCh37 |
| NC_000005.8:g.169467829G= | NCBI36 |
| NG_012068.1:g.7335G= | |
| NG_012068.2:g.7335G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_012188.5:c.773G= MANE Select | NP_036320.2:p.Gly258= |
| ENST00000306268.8:c.773G= MANE Select | ENSP00000304286.5:p.Gly258= |
| NM_012188.4:c.773G= | NP_036320.2:p.Gly258= |
| NM_144769.2:c.575-87G= | NP_658982.1:n.575-87G= |
| NM_144769.3:c.575-87G= | NP_658982.1:n.575-87G= |
| NM_144769.4:c.575-87G= | NP_658982.1:n.575-87G= |
| ENST00000306268.6:c.773G= | ENSP00000304286.5:p.Gly258= |
| ENST00000449804.3:c.575-87G= | ENSP00000415483.2:n.575-87G= |
| ENST00000449804.4:c.575-87G= | ENSP00000415483.2:n.575-87G= |