Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.186208865G= , CM000666.2:g.186208865G= | GRCh38 |
| NC_000004.11:g.187130019G= , CM000666.1:g.187130019G= | GRCh37 |
| NC_000004.10:g.187367013G= | NCBI36 |
| NG_007965.1:g.22346G= | |
| NG_012095.2:g.4887G= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000378802.5:c.1091G= MANE Select | ENSP00000368079.4:p.Gly364= | |
| ENST00000378802.4:c.1091G= | ENSP00000368079.4:p.Gly364= | |
| ENST00000502665.1:n.326G= | ||
| ENST00000507209.5:n.5789G= | ||
| ENST00000513354.5:n.181G= | ||
| NM_207352.3:c.1091G= | NP_997235.3:p.Gly364= | |
| XM_005262935.2:c.1091G= | XP_005262992.1:p.Gly364= | |
| XM_006714184.2:c.695G= | XP_006714247.1:p.Gly232= | |
| XM_005262935.4:c.1091G= | XP_005262992.1:p.Gly364= | |
| XM_017008037.1:c.695G= | XP_016863526.1:p.Gly232= | |
| NM_207352.4:c.1091G= MANE Select | NP_997235.3:p.Gly364= |