Canonical Allele Identifier: CA1591991
Gene: PCARE HGNC NCBI

Linked Data

ClinVar Variation Id: 896274
ClinVar RCV Id: RCV001138829 RCV001227713
dbSNP Id: rs201528802
ExAC: 2:29293934 G / C
gnomAD v2: 2-29293934-G-C
gnomAD v3: 2-29071068-G-C
gnomAD v4: 2-29071068-G-C
MyVariant Identifiers: chr2:g.29293934G>C (hg19) chr2:g.29071068G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29071068G>C , CM000664.2:g.29071068G>C GRCh38
NC_000002.11:g.29293934G>C , CM000664.1:g.29293934G>C GRCh37
NC_000002.10:g.29147438G>C NCBI36
NG_021427.1:g.8194C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000331664.6:c.3194C>G MANE Select ENSP00000332809.4:p.Pro1065Arg
ENST00000331664.5:c.3194C>G ENSP00000332809.4:p.Pro1065Arg
NM_001029883.2:c.3194C>G NP_001025054.1:p.Pro1065Arg
XM_011532826.1:c.3194C>G XP_011531128.1:p.Pro1065Arg
XR_939901.1:n.185+1901G>C
XR_939902.1:n.173+1913G>C
NM_001029883.3:c.3194C>G MANE Select NP_001025054.1:p.Pro1065Arg
Search 100 bp 5'
Search 100 bp 3'