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Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.111122178G= , CM000665.2:g.111122178G=
GRCh38
NC_000003.11:g.110841025G= , CM000665.1:g.110841025G=
GRCh37
NC_000003.10:g.112323715G=
NCBI36
NG_029835.1:g.55420G=
Transcript Alleles
HGVS
Amino-acid Change
ENST00000485303.6:c.857G=
MANE Select
ENSP00000418070.1:p.Gly286=
ENST00000319792.7:c.857G=
ENSP00000321514.3:p.Gly286=
ENST00000485303.5:c.857G=
ENSP00000418070.1:p.Gly286=
ENST00000486596.5:c.558G=
ENST00000493615.5:c.788G=
ENSP00000420579.1:p.Gly263=
NM_001243286.1:c.857G=
NP_001230215.1:p.Gly286=
NM_001243288.1:c.788G=
NP_001230217.1:p.Gly263=
NM_015480.2:c.857G=
NP_056295.1:p.Gly286=
XM_005247322.3:c.857G=
XP_005247379.2:p.Gly286=
XM_011512662.1:c.950G=
XP_011510964.1:p.Gly317=
XM_011512663.1:c.950G=
XP_011510965.1:p.Gly317=
XM_011512664.1:c.788G=
XP_011510966.1:p.Gly263=
XM_011512665.1:c.950G=
XP_011510967.1:p.Gly317=
XM_011512666.1:c.950G=
XP_011510968.1:p.Gly317=
XM_011512667.1:c.221G=
XP_011510969.1:p.Gly74=
XR_924122.1:n.1180G=
XM_017006123.1:c.950G=
XP_016861612.1:p.Gly317=
XM_017006124.1:c.812G=
XP_016861613.1:p.Gly271=
XM_017006125.1:c.788G=
XP_016861614.1:p.Gly263=
XM_017006126.1:c.857G=
XP_016861615.1:p.Gly286=
XM_017006127.2:c.221G=
XP_016861616.1:p.Gly74=
XR_002959508.1:n.1138G=
XR_924122.2:n.1180G=
NM_015480.3:c.857G=
MANE Select
NP_056295.1:p.Gly286=
NM_001243286.2:c.857G=
NP_001230215.1:p.Gly286=
NM_001243288.2:c.788G=
NP_001230217.1:p.Gly263=