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Genomic Alleles
HGVS
Genome Assembly
NC_000022.11:g.50074255G>C , CM000684.2:g.50074255G>C
GRCh38
NC_000022.10:g.50512684G>C , CM000684.1:g.50512684G>C
GRCh37
NC_000022.9:g.48854811G>C
NCBI36
NG_009162.1:g.16675C>G
Transcript Alleles
HGVS
Amino-acid Change
ENST00000311597.10:c.675C>G
MANE Select
ENSP00000310375.6:p.Gly225=
ENST00000311597.9:c.675C>G
ENSP00000310375.5:p.Gly225=
ENST00000395876.6:c.675C>G
ENSP00000379216.2:p.Gly225=
ENST00000442311.1:c.585C>G
ENSP00000401385.1:p.Gly195=
ENST00000470008.1:n.155C>G
NM_015166.3:c.675C>G
NP_055981.1:p.Gly225=
NM_139202.2:c.675C>G
NP_631941.1:p.Gly225=
XM_011530678.1:c.675C>G
XP_011528980.1:p.Gly225=
XR_430476.2:n.1070C>G
XM_011530678.2:c.675C>G
XP_011528980.1:p.Gly225=
XM_017028671.1:c.675C>G
XP_016884160.1:p.Gly225=
XR_001755180.2:n.1180C>G
XR_001755181.2:n.948C>G
NM_001376472.1:c.675C>G
NP_001363401.1:p.Gly225=
NM_001376473.1:c.675C>G
NP_001363402.1:p.Gly225=
NM_001376474.1:c.675C>G
NP_001363403.1:p.Gly225=
NM_001376475.1:c.675C>G
NP_001363404.1:p.Gly225=
NM_001376476.1:c.675C>G
NP_001363405.1:p.Gly225=
NM_001376477.1:c.675C>G
NP_001363406.1:p.Gly225=
NM_001376478.1:c.675C>G
NP_001363407.1:p.Gly225=
NM_001376479.1:c.675C>G
NP_001363408.1:p.Gly225=
NM_001376480.1:c.585C>G
NP_001363409.1:p.Gly195=
NM_001376481.1:c.573C>G
NP_001363410.1:p.Gly191=
NM_001376482.1:c.519C>G
NP_001363411.1:p.Gly173=
NM_001376483.1:c.519C>G
NP_001363412.1:p.Gly173=
NM_001376484.1:c.438C>G
NP_001363413.1:p.Gly146=
NM_015166.4:c.675C>G
MANE Select
NP_055981.1:p.Gly225=
NM_139202.3:c.675C>G
NP_631941.1:p.Gly225=
NR_164811.1:n.1022C>G
NR_164812.1:n.806C>G
NR_164813.1:n.1199C>G