HGVS | Genome Assembly |
---|---|
NC_000002.12:g.202467519G>C , CM000664.2:g.202467519G>C | GRCh38 |
NC_000002.11:g.203332242G>C , CM000664.1:g.203332242G>C | GRCh37 |
NC_000002.10:g.203040487G>C | NCBI36 |
NG_009363.1:g.96193G>C , LRG_712:g.96193G>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000374580.10:c.248G>C MANE Select | ENSP00000363708.4:p.Gly83Ala | |
ENST00000638587.1:c.179G>C | ENSP00000491062.1:p.Arg60Thr | |
ENST00000374574.2:c.248G>C | ENSP00000363702.2:p.Gly83Ala | |
ENST00000374580.8:c.248G>C | ENSP00000363708.4:p.Gly83Ala | |
ENST00000479069.1:n.155G>C | ||
NM_001204.6:c.248G>C , LRG_712t1:c.248G>C | NP_001195.2:p.Gly83Ala | |
XM_011511687.1:c.248G>C | XP_011509989.1:p.Gly83Ala | |
XM_011511688.1:c.248G>C | XP_011509990.1:p.Gly83Ala | |
NM_001204.7:c.248G>C MANE Select | NP_001195.2:p.Gly83Ala |