HGVS | Genome Assembly |
---|---|
NC_000007.14:g.93101422C>G , CM000669.2:g.93101422C>G | GRCh38 |
NC_000007.13:g.92730735C>G , CM000669.1:g.92730735C>G | GRCh37 |
NC_000007.12:g.92568671C>G | NCBI36 |
NG_023419.1:g.21602G>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000379958.3:c.4676G>C MANE Select | ENSP00000369292.2:p.Gly1559Ala | |
ENST00000379958.2:c.4676G>C | ENSP00000369292.2:p.Gly1559Ala | |
ENST00000620985.4:c.4676G>C | ENSP00000484636.1:p.Gly1559Ala | |
NM_001193307.1:c.4676G>C | NP_001180236.1:p.Gly1559Ala | |
NM_017654.3:c.4676G>C | NP_060124.2:p.Gly1559Ala | |
NM_017654.4:c.4676G>C MANE Select | NP_060124.2:p.Gly1559Ala | |
NM_001193307.2:c.4676G>C | NP_001180236.1:p.Gly1559Ala |