Canonical Allele Identifier: CA312866
Gene: PC HGNC NCBI

Linked Data

ClinVar Variation Id: 203902
dbSNP Id: rs56705397

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66850256A>G , CM000673.2:g.66850256A>G GRCh38
NC_000011.9:g.66617727A>G , CM000673.1:g.66617727A>G GRCh37
NC_000011.8:g.66374303A>G NCBI36
NG_008319.1:g.113121T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000393958.7:c.2682T>C ENSP00000377530.2:p.Tyr894=
ENST00000393960.7:c.2682T>C MANE Select ENSP00000377532.1:p.Tyr894=
ENST00000525476.2:n.290-191T>C
ENST00000528224.2:c.*691T>C ENSP00000498317.1:p.=
ENST00000529047.6:c.2682T>C ENSP00000435905.2:p.Tyr894=
ENST00000651036.1:c.2682T>C ENSP00000498406.1:p.Tyr894=
ENST00000651469.1:c.*1158T>C ENSP00000498712.1:p.=
ENST00000651854.1:c.2682T>C ENSP00000498994.1:p.Tyr894=
ENST00000652125.1:c.2682T>C ENSP00000498302.1:p.Tyr894=
ENST00000393955.6:c.2682T>C ENSP00000377527.2:p.Tyr894=
ENST00000393958.6:c.2682T>C ENSP00000377530.2:p.Tyr894=
ENST00000393960.5:c.2682T>C ENSP00000377532.1:p.Tyr894=
ENST00000529047.5:c.42T>C ENSP00000435905.1:p.Tyr14=
NM_000920.3:c.2682T>C NP_000911.2:p.Tyr894=
NM_001040716.1:c.2682T>C NP_001035806.1:p.Tyr894=
NM_022172.2:c.2682T>C NP_071504.2:p.Tyr894=
XM_005274031.3:c.2682T>C XP_005274088.1:p.Tyr894=
XM_005274032.3:c.2682T>C XP_005274089.1:p.Tyr894=
XM_006718577.2:c.2682T>C XP_006718640.1:p.Tyr894=
XM_006718578.2:c.2682T>C XP_006718641.1:p.Tyr894=
XM_006718579.2:c.1161T>C XP_006718642.1:p.Tyr387=
XM_011545085.1:c.2682T>C XP_011543387.1:p.Tyr894=
XM_011545086.1:c.2682T>C XP_011543388.1:p.Tyr894=
XM_011545087.1:c.1386T>C XP_011543389.1:p.Tyr462=
XM_011545088.1:c.1317T>C XP_011543390.1:p.Tyr439=
XM_005274031.4:c.2682T>C XP_005274088.1:p.Tyr894=
XM_005274032.4:c.2682T>C XP_005274089.1:p.Tyr894=
XM_006718578.3:c.2682T>C XP_006718641.1:p.Tyr894=
XM_006718579.3:c.1161T>C XP_006718642.1:p.Tyr387=
XM_011545086.2:c.2682T>C XP_011543388.1:p.Tyr894=
XM_011545087.2:c.1386T>C XP_011543389.1:p.Tyr462=
XM_017017868.1:c.2682T>C XP_016873357.1:p.Tyr894=
XM_017017869.1:c.2682T>C XP_016873358.1:p.Tyr894=
XM_017017870.1:c.2682T>C XP_016873359.1:p.Tyr894=
XM_017017871.1:c.2682T>C XP_016873360.1:p.Tyr894=
XM_017017872.2:c.2682T>C XP_016873361.1:p.Tyr894=
NM_000920.4:c.2682T>C NP_000911.2:p.Tyr894=
NM_001040716.2:c.2682T>C MANE Select NP_001035806.1:p.Tyr894=
NM_022172.3:c.2682T>C NP_071504.2:p.Tyr894=