Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.123218627G>C , CM000668.2:g.123218627G>C | GRCh38 |
| NC_000006.11:g.123539772G>C , CM000668.1:g.123539772G>C | GRCh37 |
| NC_000006.10:g.123581471G>C | NCBI36 |
| NG_030438.1:g.423467C>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_006073.4:c.2164C>G MANE Select | NP_006064.2:p.Pro722Ala |
| ENST00000334268.9:c.2164C>G MANE Select | ENSP00000333984.5:p.Pro722Ala |
| NM_006073.3:c.2164C>G | NP_006064.2:p.Pro722Ala |
| ENST00000334268.8:c.2164C>G | ENSP00000333984.5:p.Pro722Ala |
| XM_011535382.1:c.2083C>G | XP_011533684.1:p.Pro695Ala |