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Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.186280371C>G , CM000666.2:g.186280371C>G
GRCh38
NC_000004.11:g.187201525C>G , CM000666.1:g.187201525C>G
GRCh37
NC_000004.10:g.187438519C>G
NCBI36
NG_008051.1:g.19408C>G , LRG_583:g.19408C>G
Transcript Alleles
HGVS
Amino-acid Change
ENST00000403665.7:c.1014C>G
MANE Select
ENSP00000384957.2:p.Ser338=
ENST00000264692.8:c.852C>G
ENSP00000264692.5:p.Ser284=
ENST00000403665.6:c.1014C>G
ENSP00000384957.2:p.Ser338=
ENST00000452239.1:c.461C>G
NM_000128.3:c.1014C>G , LRG_583t1:c.1014C>G
NP_000119.1:p.Ser338=
XM_005262821.2:c.1014C>G
XP_005262878.1:p.Ser338=
XM_005262822.2:c.1014C>G
XP_005262879.1:p.Ser338=
XM_005262823.2:c.744C>G
XP_005262880.1:p.Ser248=
XM_005262824.1:c.1014C>G
XP_005262881.1:p.Ser338=
XM_006714137.1:c.966C>G
XP_006714200.1:p.Ser322=
XR_938706.1:n.1366C>G
XR_938707.1:n.1366C>G
XM_005262821.4:c.1014C>G
XP_005262878.1:p.Ser338=
XM_005262822.4:c.1014C>G
XP_005262879.1:p.Ser338=
XM_005262823.4:c.744C>G
XP_005262880.1:p.Ser248=
XM_006714137.3:c.966C>G
XP_006714200.1:p.Ser322=
XM_017007884.2:c.1014C>G
XP_016863373.1:p.Ser338=
XM_017007885.2:c.1014C>G
XP_016863374.1:p.Ser338=
XM_017007886.2:c.1014C>G
XP_016863375.1:p.Ser338=
XR_001741172.2:n.1347C>G
NM_000128.4:c.1014C>G
MANE Select
NP_000119.1:p.Ser338=