HGVS | Genome Assembly |
---|---|
NC_000008.11:g.6877802G>C , CM000670.2:g.6877802G>C | GRCh38 |
NC_000008.10:g.6735324G>C , CM000670.1:g.6735324G>C | GRCh37 |
NC_000008.9:g.6722734G>C | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000297439.4:c.56C>G MANE Select | ENSP00000297439.3:p.Ala19Gly | |
ENST00000297439.3:c.56C>G | ENSP00000297439.3:p.Ala19Gly | |
NM_005218.3:c.56C>G | NP_005209.1:p.Ala19Gly | |
NM_005218.4:c.56C>G MANE Select | NP_005209.1:p.Ala19Gly |