HGVS | Genome Assembly |
---|---|
NC_000023.11:g.22032909A>G , CM000685.2:g.22032909A>G | GRCh38 |
NC_000023.10:g.22051027A>G , CM000685.1:g.22051027A>G | GRCh37 |
NC_000023.9:g.21960948A>G | NCBI36 |
NG_007563.2:g.5107A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000475778.2:n.330A>G | ||
ENST00000683214.1:n.330A>G | ||
ENST00000684143.1:c.-97A>G | ENSP00000508264.1:n.-97A>G | |
ENST00000379374.5:c.-97A>G MANE Select | ENSP00000368682.4:n.-97A>G | |
ENST00000379374.4:c.-97A>G | ENSP00000368682.4:n.-97A>G | |
NM_000444.5:c.-97A>G | NP_000435.3:n.-97A>G | |
NM_001282754.1:c.-97A>G | NP_001269683.1:n.-97A>G | |
XM_011545535.1:c.-97A>G | XP_011543837.1:n.-97A>G | |
XR_001755695.1:n.583A>G | ||
NM_000444.6:c.-97A>G MANE Select | NP_000435.3:n.-97A>G | |
NM_001282754.2:c.-97A>G | NP_001269683.1:n.-97A>G |