HGVS | Genome Assembly |
---|---|
NC_000011.10:g.89178548G>C , CM000673.2:g.89178548G>C | GRCh38 |
NC_000011.9:g.88911716G>C , CM000673.1:g.88911716G>C | GRCh37 |
NC_000011.8:g.88551364G>C | NCBI36 |
NG_008748.1:g.5677G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000263321.6:c.595G>C MANE Select | ENSP00000263321.4:p.Asp199His | |
ENST00000263321.5:c.595G>C | ENSP00000263321.4:p.Asp199His | |
ENST00000526139.1:n.656G>C | ||
NM_000372.4:c.595G>C | NP_000363.1:p.Asp199His | |
XM_011542970.1:c.595G>C | XP_011541272.1:p.Asp199His | |
XM_011542970.2:c.595G>C | XP_011541272.1:p.Asp199His | |
XR_001748321.1:n.2718-65015C>G | ||
XR_001748322.1:n.2733-65015C>G | ||
NM_000372.5:c.595G>C MANE Select | NP_000363.1:p.Asp199His |