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Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.65982119C= , CM000669.2:g.65982119C=
GRCh38
NC_000007.13:g.65447106C= , CM000669.1:g.65447106C=
GRCh37
NC_000007.12:g.65084541C=
NCBI36
NG_016197.1:g.5196G=
Transcript Alleles
HGVS
Amino-acid Change
ENST00000304895.9:c.65G=
MANE Select
ENSP00000302728.4:p.Gly22=
ENST00000304895.8:c.65G=
ENSP00000302728.4:p.Gly22=
ENST00000421103.5:c.65G=
ENSP00000391390.1:p.Gly22=
ENST00000430730.5:c.65G=
ENSP00000411859.1:p.Gly22=
ENST00000446111.1:c.65G=
ENSP00000416793.1:p.Gly22=
ENST00000447929.5:c.65G=
ENSP00000411262.1:p.Gly22=
NM_000181.3:c.65G=
NP_000172.2:p.Gly22=
NM_001284290.1:c.65G=
NP_001271219.1:p.Gly22=
NM_001293104.1:c.-321G=
NP_001280033.1:n.-321G=
NM_001293105.1:c.-265G=
NP_001280034.1:n.-265G=
NR_120531.1:n.196G=
XM_005250297.3:c.65G=
XP_005250354.1:p.Gly22=
XM_011516113.1:c.-265G=
XP_011514415.1:n.-265G=
XR_927461.1:n.191G=
XM_005250297.4:c.65G=
XP_005250354.1:p.Gly22=
XM_011516114.2:c.-621G=
XP_011514416.1:n.-621G=
XM_017012091.1:c.-265G=
XP_016867580.1:n.-265G=
XM_017012092.1:c.-321G=
XP_016867581.1:n.-321G=
XM_017012093.2:c.-621G=
XP_016867582.1:n.-621G=
XR_001744658.2:n.110G=
XR_001744659.2:n.110G=
XR_001744660.2:n.110G=
XR_001744661.2:n.110G=
XR_927461.3:n.110G=
NM_000181.4:c.65G=
MANE Select
NP_000172.2:p.Gly22=
NM_001284290.2:c.65G=
NP_001271219.1:p.Gly22=
NM_001293104.2:c.-321G=
NP_001280033.1:n.-321G=
NM_001293105.2:c.-265G=
NP_001280034.1:n.-265G=
NR_120531.2:n.95G=