Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.44376320A>G , CM000679.2:g.44376320A>G | GRCh38 |
| NC_000017.10:g.42453688A>G , CM000679.1:g.42453688A>G | GRCh37 |
| NC_000017.9:g.39809214A>G | NCBI36 |
| NG_008331.1:g.18186T>C , LRG_479:g.18186T>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000419.5:c.2336T>C MANE Select | NP_000410.2:p.Val779Ala |
| ENST00000262407.6:c.2336T>C MANE Select | ENSP00000262407.5:p.Val779Ala |
| NM_000419.3:c.2336T>C , LRG_479t1:c.2336T>C | NP_000410.2:p.Val779Ala |
| NM_000419.4:c.2336T>C | NP_000410.2:p.Val779Ala |
| ENST00000262407.5:c.2336T>C | ENSP00000262407.5:p.Val779Ala |
| ENST00000592462.5:n.1131T>C | |
| ENST00000648408.1:c.1767T>C | |
| XM_011524749.1:c.2336T>C | XP_011523051.1:p.Val779Ala |
| XM_011524750.1:c.2336T>C | XP_011523052.1:p.Val779Ala |