Canonical Allele Identifier: CA341754
Gene: PC HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 21222
dbSNP Id: rs113994145

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66851880C>T , CM000673.2:g.66851880C>T GRCh38
NC_000011.8:g.66375927C>T NCBI36
NC_000011.9:g.66619351C>T , CM000673.1:g.66619351C>T GRCh37
NG_008319.1:g.111497G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000393955.6:c.1892G>A ENSP00000377527.2:p.Arg631Gln
ENST00000393958.6:c.1892G>A ENSP00000377530.2:p.Arg631Gln
ENST00000393960.5:c.1892G>A ENSP00000377532.1:p.Arg631Gln
ENST00000530259.1:n.505G>A
NM_000920.3:c.1892G>A VV NP_000911.2:p.Arg631Gln
NM_001040716.1:c.1892G>A VV NP_001035806.1:p.Arg631Gln
NM_022172.2:c.1892G>A VV NP_071504.2:p.Arg631Gln
XM_005274031.3:c.1892G>A XP_005274088.1:p.Arg631Gln
XM_005274032.3:c.1892G>A XP_005274089.1:p.Arg631Gln
XM_006718577.2:c.1892G>A XP_006718640.1:p.Arg631Gln
XM_006718578.2:c.1892G>A XP_006718641.1:p.Arg631Gln
XM_006718579.2:c.371G>A XP_006718642.1:p.Arg124Gln
XM_011545085.1:c.1892G>A XP_011543387.1:p.Arg631Gln
XM_011545086.1:c.1892G>A XP_011543388.1:p.Arg631Gln
XM_011545087.1:c.596G>A XP_011543389.1:p.Arg199Gln
XM_011545088.1:c.527G>A XP_011543390.1:p.Arg176Gln