Canonical Allele Identifier: CA408710726
Gene: PROCR HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.33764569G>C (hg19) chr20:g.35176766G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.35176766G>C , CM000682.2:g.35176766G>C GRCh38
NC_000020.10:g.33764569G>C , CM000682.1:g.33764569G>C GRCh37
NC_000020.9:g.33228230G>C NCBI36
NG_032899.1:g.9796G>C
NG_032899.2:g.9796G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000216968.5:c.670G>C MANE Select ENSP00000216968.3:p.Gly224Arg
ENST00000216968.4:c.670G>C ENSP00000216968.3:p.Gly224Arg
ENST00000634509.1:c.94+320G>C ENSP00000489456.1:n.94+320G>C
ENST00000635377.1:c.502-321G>C
NM_006404.4:c.670G>C NP_006395.2:p.Gly224Arg
XM_011528496.1:c.601+320G>C XP_011526798.1:n.601+320G>C
NM_001355008.1:c.-101-10895C>G NP_001341937.1:n.-101-10895C>G
NM_006404.5:c.670G>C MANE Select NP_006395.2:p.Gly224Arg
NM_001355008.2:c.-101-10895C>G NP_001341937.1:n.-101-10895C>G
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