Canonical Allele Identifier: CA9830371
Gene: PROCR HGNC NCBI

Linked Data

dbSNP Id: rs867186

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.35176751A>G , CM000682.2:g.35176751A>G GRCh38
NC_000020.10:g.33764554A>G , CM000682.1:g.33764554A>G GRCh37
NC_000020.9:g.33228215A>G NCBI36
NG_032899.1:g.9781A>G
NG_032899.2:g.9781A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000216968.5:c.655A>G MANE Select ENSP00000216968.3:p.Ser219Gly
ENST00000216968.4:c.655A>G ENSP00000216968.3:p.Ser219Gly
ENST00000634509.1:n.94+305A>G ENSP00000489456.1:p.=
ENST00000635377.1:n.501+305A>G
NM_006404.4:c.655A>G NP_006395.2:p.Ser219Gly
XM_011528496.1:c.601+305A>G XP_011526798.1:p.=
NM_001355008.1:c.-101-10880T>C NP_001341937.1:p.=
NM_006404.5:c.655A>G MANE Select NP_006395.2:p.Ser219Gly
NM_001355008.2:c.-101-10880T>C NP_001341937.1:p.=