HGVS | Genome Assembly |
---|---|
NC_000017.11:g.42536334C>G , CM000679.2:g.42536334C>G | GRCh38 |
NC_000017.10:g.40688352C>G , CM000679.1:g.40688352C>G | GRCh37 |
NC_000017.9:g.37941878C>G | NCBI36 |
NG_011552.1:g.5402C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000225927.7:c.62C>G MANE Select | ENSP00000225927.1:p.Ala21Gly | |
ENST00000225927.6:c.62C>G | ENSP00000225927.1:p.Ala21Gly | |
NM_000263.3:c.62C>G | NP_000254.2:p.Ala21Gly | |
XM_024450771.1:c.62C>G | XP_024306539.1:p.Ala21Gly | |
NM_000263.4:c.62C>G MANE Select | NP_000254.2:p.Ala21Gly |