Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.66956459T= , CM000669.2:g.66956459T= | GRCh38 |
| NC_000007.13:g.66421446T= , CM000669.1:g.66421446T= | GRCh37 |
| NC_000007.12:g.66058881T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000341567.8:c.*937T= MANE Select | ENSP00000340668.4:n.*937T= | |
| NM_017994.4:c.*937T= | NP_060464.1:n.*937T= | |
| XM_005250482.2:c.*937T= | XP_005250539.1:n.*937T= | |
| XM_005250482.4:c.*937T= | XP_005250539.1:n.*937T= | |
| XM_024446819.1:c.*937T= | XP_024302587.1:n.*937T= | |
| XM_024446820.1:c.*937T= | XP_024302588.1:n.*937T= | |
| XM_024446821.1:c.*937T= | XP_024302589.1:n.*937T= | |
| XM_024446822.1:c.*937T= | XP_024302590.1:n.*937T= | |
| NM_017994.5:c.*937T= MANE Select | NP_060464.1:n.*937T= |