Canonical Allele Identifier: CA510296719
Gene: PROCR HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.33764571T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.35176768T>G , CM000682.2:g.35176768T>G GRCh38
NC_000020.10:g.33764571T>G , CM000682.1:g.33764571T>G GRCh37
NC_000020.9:g.33228232T>G NCBI36
NG_032899.1:g.9798T>G
NG_032899.2:g.9798T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000216968.5:c.672T>G MANE Select ENSP00000216968.3:p.Gly224=
ENST00000216968.4:c.672T>G ENSP00000216968.3:p.Gly224=
ENST00000634509.1:c.94+322T>G ENSP00000489456.1:n.94+322T>G
ENST00000635377.1:c.502-319T>G
NM_006404.4:c.672T>G NP_006395.2:p.Gly224=
XM_011528496.1:c.601+322T>G XP_011526798.1:n.601+322T>G
NM_001355008.1:c.-101-10897A>C NP_001341937.1:n.-101-10897A>C
NM_006404.5:c.672T>G MANE Select NP_006395.2:p.Gly224=
NM_001355008.2:c.-101-10897A>C NP_001341937.1:n.-101-10897A>C
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