HGVS | Genome Assembly |
---|---|
NC_000002.12:g.240872984A>G , CM000664.2:g.240872984A>G | GRCh38 |
NC_000002.11:g.241812401A>G , CM000664.1:g.241812401A>G | GRCh37 |
NC_000002.10:g.241461074A>G | NCBI36 |
NG_008005.1:g.9240A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307503.4:c.530A>G MANE Select | ENSP00000302620.3:p.Lys177Arg | |
ENST00000307503.3:c.530A>G | ENSP00000302620.3:p.Lys177Arg | |
ENST00000472436.1:n.550A>G | ||
ENST00000476698.1:n.267A>G | ||
NM_000030.2:c.530A>G | NP_000021.1:p.Lys177Arg | |
NM_000030.3:c.530A>G MANE Select | NP_000021.1:p.Lys177Arg |