Canonical Allele Identifier: CA1017161588
Gene: PROCR HGNC NCBI

Linked Data

dbSNP Id: rs1600734651
gnomAD v3: 20-35175999-A-C
gnomAD v4: 20-35175999-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.35175999A>C , CM000682.2:g.35175999A>C GRCh38
NC_000020.10:g.33763802A>C , CM000682.1:g.33763802A>C GRCh37
NC_000020.9:g.33227463A>C NCBI36
NG_032899.1:g.9029A>C
NG_032899.2:g.9029A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000216968.5:c.323-169A>C MANE Select ENSP00000216968.3:n.323-169A>C
ENST00000216968.4:c.323-169A>C ENSP00000216968.3:n.323-169A>C
ENST00000635377.1:c.223-169A>C
NM_006404.4:c.323-169A>C NP_006395.2:n.323-169A>C
XM_011528496.1:c.323-169A>C XP_011526798.1:n.323-169A>C
NM_001355008.1:c.-101-10128T>G NP_001341937.1:n.-101-10128T>G
NM_006404.5:c.323-169A>C MANE Select NP_006395.2:n.323-169A>C
NM_001355008.2:c.-101-10128T>G NP_001341937.1:n.-101-10128T>G
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