Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.94415263G>C , CM000669.2:g.94415263G>C | GRCh38 |
| NC_000007.13:g.94044575G>C , CM000669.1:g.94044575G>C | GRCh37 |
| NC_000007.12:g.93882511G>C | NCBI36 |
| NG_007405.1:g.25703G>C , LRG_2:g.25703G>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000297268.11:c.1757G>C MANE Select | ENSP00000297268.6:p.Gly586Ala | |
| ENST00000297268.10:c.1757G>C | ENSP00000297268.6:p.Gly586Ala | |
| ENST00000473573.5:n.94G>C | ||
| ENST00000488298.5:n.181G>C | ||
| ENST00000620463.1:c.1751G>C | ENSP00000477719.1:p.Gly584Ala | |
| NM_000089.3:c.1757G>C , LRG_2t1:c.1757G>C | NP_000080.2:p.Gly586Ala | |
| NM_000089.4:c.1757G>C MANE Select | NP_000080.2:p.Gly586Ala |