HGVS | Genome Assembly |
---|---|
NC_000001.11:g.186172058C>G , CM000663.2:g.186172058C>G | GRCh38 |
NC_000001.10:g.186141190C>G , CM000663.1:g.186141190C>G | GRCh37 |
NC_000001.9:g.184407813C>G | NCBI36 |
NG_011841.1:g.442508C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000271588.9:c.15741C>G MANE Select | ENSP00000271588.4:p.Asn5247Lys | |
ENST00000271588.8:c.15741C>G | ENSP00000271588.4:p.Asn5247Lys | |
ENST00000414277.1:c.117C>G | ENSP00000406205.1:p.Asn39Lys | |
ENST00000475585.1:n.329C>G | ||
NM_031935.2:c.15741C>G | NP_114141.2:p.Asn5247Lys | |
XM_011510037.1:c.15456C>G | XP_011508339.1:p.Asn5152Lys | |
XM_011510038.1:c.15741C>G | XP_011508340.1:p.Asn5247Lys | |
XM_011510038.3:c.15741C>G | XP_011508340.1:p.Asn5247Lys | |
XM_017002437.1:c.13764C>G | XP_016857926.1:p.Asn4588Lys | |
NM_031935.3:c.15741C>G MANE Select | NP_114141.2:p.Asn5247Lys |