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Genomic Alleles
HGVS
Genome Assembly
NC_000023.11:g.108622766G= , CM000685.2:g.108622766G=
GRCh38
NC_000023.10:g.107865996G= , CM000685.1:g.107865996G=
GRCh37
NC_000023.9:g.107752652G=
NCBI36
NG_011977.1:g.187843G=
NG_011977.2:g.187843G=
Transcript Alleles
HGVS
Amino-acid Change
ENST00000328300.11:c.2858G=
MANE Select
ENSP00000331902.7:p.Gly953=
ENST00000361603.7:c.2858G=
ENSP00000354505.2:p.Gly953=
ENST00000328300.10:c.2858G=
ENSP00000331902.6:p.Gly953=
ENST00000361603.6:c.2858G=
ENSP00000354505.2:p.Gly953=
ENST00000483338.1:n.2314G=
ENST00000505728.1:c.91G=
NM_000495.4:c.2858G=
NP_000486.1:p.Gly953=
NM_033380.2:c.2858G=
NP_203699.1:p.Gly953=
XM_005262070.2:c.2858G=
XP_005262127.1:p.Gly953=
XM_005262072.3:c.2858G=
XP_005262129.1:p.Gly953=
XM_006724616.2:c.2858G=
XP_006724679.1:p.Gly953=
XM_011530849.1:c.2534G=
XP_011529151.1:p.Gly845=
XM_011530850.1:c.2858G=
XP_011529152.1:p.Gly953=
XM_011530851.1:c.431G=
XP_011529153.1:p.Gly144=
XM_011530849.2:c.2873G=
XP_011529151.2:p.Gly958=
XM_017029259.2:c.2873G=
XP_016884748.1:p.Gly958=
XM_017029260.1:c.2873G=
XP_016884749.1:p.Gly958=
XM_017029261.1:c.2873G=
XP_016884750.1:p.Gly958=
XM_017029262.2:c.2873G=
XP_016884751.1:p.Gly958=
XM_017029263.2:c.1193G=
XP_016884752.1:p.Gly398=
NM_000495.5:c.2858G=
NP_000486.1:p.Gly953=
NM_033380.3:c.2858G=
MANE Select
NP_203699.1:p.Gly953=