Canonical Allele Identifier: CA510296761
Gene: PROCR HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.33764577T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.35176774T>C , CM000682.2:g.35176774T>C GRCh38
NC_000020.10:g.33764577T>C , CM000682.1:g.33764577T>C GRCh37
NC_000020.9:g.33228238T>C NCBI36
NG_032899.1:g.9804T>C
NG_032899.2:g.9804T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000216968.5:c.678T>C MANE Select ENSP00000216968.3:p.Ala226=
ENST00000216968.4:c.678T>C ENSP00000216968.3:p.Ala226=
ENST00000634509.1:c.94+328T>C ENSP00000489456.1:n.94+328T>C
ENST00000635377.1:c.502-313T>C
NM_006404.4:c.678T>C NP_006395.2:p.Ala226=
XM_011528496.1:c.601+328T>C XP_011526798.1:n.601+328T>C
NM_001355008.1:c.-101-10903A>G NP_001341937.1:n.-101-10903A>G
NM_006404.5:c.678T>C MANE Select NP_006395.2:p.Ala226=
NM_001355008.2:c.-101-10903A>G NP_001341937.1:n.-101-10903A>G
Search 100 bp 5'
Search 100 bp 3'