Canonical Allele Identifier: CA635336372
Gene: PROCR HGNC NCBI

Linked Data

gnomAD v2: 20-33763520-T-A
MyVariant Identifiers: chr20:g.33763520T>A (hg19) chr20:g.35175717T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.35175717T>A , CM000682.2:g.35175717T>A GRCh38
NC_000020.10:g.33763520T>A , CM000682.1:g.33763520T>A GRCh37
NC_000020.9:g.33227181T>A NCBI36
NG_032899.1:g.8747T>A
NG_032899.2:g.8747T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000216968.5:c.323-451T>A MANE Select ENSP00000216968.3:n.323-451T>A
ENST00000216968.4:c.323-451T>A ENSP00000216968.3:n.323-451T>A
ENST00000635377.1:c.223-451T>A
NM_006404.4:c.323-451T>A NP_006395.2:n.323-451T>A
XM_011528496.1:c.323-451T>A XP_011526798.1:n.323-451T>A
NM_001355008.1:c.-101-9846A>T NP_001341937.1:n.-101-9846A>T
NM_006404.5:c.323-451T>A MANE Select NP_006395.2:n.323-451T>A
NM_001355008.2:c.-101-9846A>T NP_001341937.1:n.-101-9846A>T
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