HGVS | Genome Assembly |
---|---|
NC_000002.12:g.202531035G= , CM000664.2:g.202531035G= | GRCh38 |
NC_000002.11:g.203395758G= , CM000664.1:g.203395758G= | GRCh37 |
NC_000002.10:g.203104003G= | NCBI36 |
NG_009363.1:g.159709G= , LRG_712:g.159709G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000374580.10:c.1128+81G= MANE Select | ENSP00000363708.4:n.1128+81G= | |
ENST00000638587.1:c.1059+81G= | ENSP00000491062.1:n.1059+81G= | |
ENST00000374574.2:c.1128+81G= | ENSP00000363702.2:n.1128+81G= | |
ENST00000374580.8:c.1128+81G= | ENSP00000363708.4:n.1128+81G= | |
NM_001204.6:c.1128+81G= , LRG_712t1:c.1128+81G= | NP_001195.2:n.1128+81G= | |
XM_011511687.1:c.1128+81G= | XP_011509989.1:n.1128+81G= | |
XM_011511688.1:c.1128+81G= | XP_011509990.1:n.1128+81G= | |
NM_001204.7:c.1128+81G= MANE Select | NP_001195.2:n.1128+81G= |