Canonical Allele Identifier: CA221425
Gene: PCARE HGNC NCBI

Linked Data

ClinVar Variation Id: 93473
ClinVar RCV Id: RCV000079371
dbSNP Id: rs398123539
ExAC: 2:29294174 T / C
gnomAD v2: 2-29294174-T-C
gnomAD v3: 2-29071308-T-C
gnomAD v4: 2-29071308-T-C
MyVariant Identifiers: chr2:g.29294174T>C (hg19) chr2:g.29071308T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29071308T>C , CM000664.2:g.29071308T>C GRCh38
NC_000002.11:g.29294174T>C , CM000664.1:g.29294174T>C GRCh37
NC_000002.10:g.29147678T>C NCBI36
NG_021427.1:g.7954A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000331664.6:c.2954A>G MANE Select ENSP00000332809.4:p.Glu985Gly
ENST00000331664.5:c.2954A>G ENSP00000332809.4:p.Glu985Gly
NM_001029883.2:c.2954A>G NP_001025054.1:p.Glu985Gly
XM_011532826.1:c.2954A>G XP_011531128.1:p.Glu985Gly
XR_939901.1:n.185+2141T>C
XR_939902.1:n.173+2153T>C
NM_001029883.3:c.2954A>G MANE Select NP_001025054.1:p.Glu985Gly
Search 100 bp 5'
Search 100 bp 3'