Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.241850169C= , CM000664.2:g.241850169C= | GRCh38 |
| NC_000002.11:g.242792321C= , CM000664.1:g.242792321C= | GRCh37 |
| NC_000002.10:g.242440994C= | NCBI36 |
| NG_012110.1:g.13738G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005018.3:c.*889G= MANE Select | NP_005009.2:n.*889G= |
| ENST00000334409.10:c.*889G= MANE Select | ENSP00000335062.5:n.*889G= |
| NM_005018.2:c.*889G= | NP_005009.2:n.*889G= |
| ENST00000334409.9:c.*889G= | ENSP00000335062.5:n.*889G= |
| XM_017004293.1:c.*889G= | XP_016859782.1:n.*889G= |