Canonical Allele Identifier: CA1017161492
Gene: PROCR HGNC NCBI

Linked Data

dbSNP Id: rs960680652
gnomAD v3: 20-35175839-C-A
gnomAD v4: 20-35175839-C-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.35175839C>A , CM000682.2:g.35175839C>A GRCh38
NC_000020.10:g.33763642C>A , CM000682.1:g.33763642C>A GRCh37
NC_000020.9:g.33227303C>A NCBI36
NG_032899.1:g.8869C>A
NG_032899.2:g.8869C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000216968.5:c.323-329C>A MANE Select ENSP00000216968.3:n.323-329C>A
ENST00000216968.4:c.323-329C>A ENSP00000216968.3:n.323-329C>A
ENST00000635377.1:c.223-329C>A
NM_006404.4:c.323-329C>A NP_006395.2:n.323-329C>A
XM_011528496.1:c.323-329C>A XP_011526798.1:n.323-329C>A
NM_001355008.1:c.-101-9968G>T NP_001341937.1:n.-101-9968G>T
NM_006404.5:c.323-329C>A MANE Select NP_006395.2:n.323-329C>A
NM_001355008.2:c.-101-9968G>T NP_001341937.1:n.-101-9968G>T
Search 100 bp 5'
Search 100 bp 3'