HGVS | Genome Assembly |
---|---|
NC_000016.10:g.28845473A>C , CM000678.2:g.28845473A>C | GRCh38 |
NC_000016.9:g.28856794A>C , CM000678.1:g.28856794A>C | GRCh37 |
NC_000016.8:g.28764295A>C | NCBI36 |
NG_008964.1:g.5936T>G | |
NG_029706.2:g.3874A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000313511.8:c.255T>G MANE Select | ENSP00000322439.3:p.Ala85= | |
ENST00000313511.7:c.255T>G | ENSP00000322439.3:p.Ala85= | |
ENST00000565012.1:c.248-418T>G | ENSP00000455007.1:n.248-418T>G | |
NM_003321.4:c.255T>G | NP_003312.3:p.Ala85= | |
XM_011545928.1:c.255T>G | XP_011544230.1:p.Ala85= | |
NM_001365360.1:c.255T>G | NP_001352289.1:p.Ala85= | |
NM_003321.5:c.255T>G MANE Select | NP_003312.3:p.Ala85= | |
NM_001365360.2:c.255T>G | NP_001352289.1:p.Ala85= |