HGVS | Genome Assembly |
---|---|
NC_000002.12:g.202559700T>C , CM000664.2:g.202559700T>C | GRCh38 |
NC_000002.11:g.203424423T>C , CM000664.1:g.203424423T>C | GRCh37 |
NC_000002.10:g.203132668T>C | NCBI36 |
NG_009363.1:g.188374T>C , LRG_712:g.188374T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000374580.10:c.2871T>C MANE Select | ENSP00000363708.4:p.Gly957= | |
ENST00000638587.1:c.2802T>C | ENSP00000491062.1:n.2802T>C | |
ENST00000374574.2:c.1591T>C | ENSP00000363702.2:p.Ter531Arg | |
ENST00000374580.8:c.2871T>C | ENSP00000363708.4:p.Gly957= | |
NM_001204.6:c.2871T>C , LRG_712t1:c.2871T>C | NP_001195.2:p.Gly957= | |
XM_011511687.1:c.2868T>C | XP_011509989.1:p.Ser956= | |
XM_011511688.1:c.1591T>C | XP_011509990.1:p.Ter531Arg | |
NM_001204.7:c.2871T>C MANE Select | NP_001195.2:p.Gly957= |