Canonical Allele Identifier: CA510296734
Gene: PROCR HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.33764574G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.35176771G>C , CM000682.2:g.35176771G>C GRCh38
NC_000020.10:g.33764574G>C , CM000682.1:g.33764574G>C GRCh37
NC_000020.9:g.33228235G>C NCBI36
NG_032899.1:g.9801G>C
NG_032899.2:g.9801G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000216968.5:c.675G>C MANE Select ENSP00000216968.3:p.Val225=
ENST00000216968.4:c.675G>C ENSP00000216968.3:p.Val225=
ENST00000634509.1:c.94+325G>C ENSP00000489456.1:n.94+325G>C
ENST00000635377.1:c.502-316G>C
NM_006404.4:c.675G>C NP_006395.2:p.Val225=
XM_011528496.1:c.601+325G>C XP_011526798.1:n.601+325G>C
NM_001355008.1:c.-101-10900C>G NP_001341937.1:n.-101-10900C>G
NM_006404.5:c.675G>C MANE Select NP_006395.2:p.Val225=
NM_001355008.2:c.-101-10900C>G NP_001341937.1:n.-101-10900C>G
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