HGVS | Genome Assembly |
---|---|
NC_000005.10:g.96416100T>G , CM000667.2:g.96416100T>G | GRCh38 |
NC_000005.9:g.95751804T>G , CM000667.1:g.95751804T>G | GRCh37 |
NC_000005.8:g.95777560T>G | NCBI36 |
NG_021161.1:g.22182A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000311106.8:c.642A>C MANE Select | ENSP00000308024.2:p.Gly214= | |
ENST00000311106.7:c.642A>C | ENSP00000308024.2:p.Gly214= | |
ENST00000508626.5:c.501A>C | ENSP00000421600.1:p.Gly167= | |
NM_000439.4:c.642A>C | NP_000430.3:p.Gly214= | |
NM_001177875.1:c.501A>C | NP_001171346.1:p.Gly167= | |
NR_130776.1:n.354+36448T>G | ||
NM_000439.5:c.642A>C MANE Select | NP_000430.3:p.Gly214= | |
NM_001177875.2:c.501A>C | NP_001171346.1:p.Gly167= |