HGVS | Genome Assembly |
---|---|
NC_000002.12:g.240878786G= , CM000664.2:g.240878786G= | GRCh38 |
NC_000002.11:g.241818203G= , CM000664.1:g.241818203G= | GRCh37 |
NC_000002.10:g.241466876G= | NCBI36 |
NG_008005.1:g.15042G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307503.4:c.1144G= MANE Select | ENSP00000302620.3:p.Ala382= | |
ENST00000307503.3:c.1144G= | ENSP00000302620.3:p.Ala382= | |
ENST00000470255.1:n.922G= | ||
NM_000030.2:c.1144G= | NP_000021.1:p.Ala382= | |
NM_000030.3:c.1144G= MANE Select | NP_000021.1:p.Ala382= |