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Genomic Alleles
HGVS
Genome Assembly
NC_000023.11:g.108620353C= , CM000685.2:g.108620353C=
GRCh38
NC_000023.10:g.107863583C= , CM000685.1:g.107863583C=
GRCh37
NC_000023.9:g.107750239C=
NCBI36
NG_011977.1:g.185430C=
NG_011977.2:g.185430C=
Transcript Alleles
HGVS
Amino-acid Change
ENST00000328300.11:c.2604C=
MANE Select
ENSP00000331902.7:p.Pro868=
ENST00000361603.7:c.2604C=
ENSP00000354505.2:p.Pro868=
ENST00000328300.10:c.2604C=
ENSP00000331902.6:p.Pro868=
ENST00000361603.6:c.2604C=
ENSP00000354505.2:p.Pro868=
ENST00000483338.1:n.2060C=
NM_000495.4:c.2604C=
NP_000486.1:p.Pro868=
NM_033380.2:c.2604C=
NP_203699.1:p.Pro868=
XM_005262070.2:c.2604C=
XP_005262127.1:p.Pro868=
XM_005262072.3:c.2604C=
XP_005262129.1:p.Pro868=
XM_006724616.2:c.2604C=
XP_006724679.1:p.Pro868=
XM_011530849.1:c.2280C=
XP_011529151.1:p.Pro760=
XM_011530850.1:c.2604C=
XP_011529152.1:p.Pro868=
XM_011530851.1:c.177C=
XP_011529153.1:p.Pro59=
XM_011530849.2:c.2619C=
XP_011529151.2:p.Pro873=
XM_017029259.2:c.2619C=
XP_016884748.1:p.Pro873=
XM_017029260.1:c.2619C=
XP_016884749.1:p.Pro873=
XM_017029261.1:c.2619C=
XP_016884750.1:p.Pro873=
XM_017029262.2:c.2619C=
XP_016884751.1:p.Pro873=
XM_017029263.2:c.939C=
XP_016884752.1:p.Pro313=
NM_000495.5:c.2604C=
NP_000486.1:p.Pro868=
NM_033380.3:c.2604C=
MANE Select
NP_203699.1:p.Pro868=