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Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.128911732C>G , CM000673.2:g.128911732C>G
GRCh38
NC_000011.9:g.128781627C>G , CM000673.1:g.128781627C>G
GRCh37
NC_000011.8:g.128286837C>G
NCBI36
NG_023406.2:g.25315C>G , LRG_333:g.25315C>G
Transcript Alleles
HGVS
Amino-acid Change
ENST00000529694.6:c.459C>G
MANE Select
ENSP00000433295.1:p.Gly153=
ENST00000338350.4:c.459C>G
ENSP00000339960.4:p.Gly153=
ENST00000529694.5:c.459C>G
ENSP00000433295.1:p.Gly153=
ENST00000533599.1:c.459C>G
ENSP00000434266.1:p.Gly153=
NM_000890.3:c.459C>G , LRG_333t1:c.459C>G
NP_000881.3:p.Gly153=
XM_011542809.1:c.459C>G
XP_011541111.1:p.Gly153=
XM_011542810.1:c.459C>G
XP_011541112.1:p.Gly153=
NM_000890.4:c.459C>G
NP_000881.3:p.Gly153=
NM_001354169.1:c.459C>G
NP_001341098.1:p.Gly153=
XM_011542809.2:c.459C>G
XP_011541111.1:p.Gly153=
XM_011542810.3:c.459C>G
XP_011541112.1:p.Gly153=
NM_000890.5:c.459C>G
MANE Select
NP_000881.3:p.Gly153=
NM_001354169.2:c.459C>G
NP_001341098.1:p.Gly153=