Canonical Allele Identifier: CA1591906
Gene: PCARE HGNC NCBI

Linked Data

ClinVar Variation Id: 752211
ClinVar RCV Id: RCV000929335 RCV001136591 RCV003890082
dbSNP Id: rs182812191
ExAC: 2:29293601 T / C
gnomAD v2: 2-29293601-T-C
gnomAD v3: 2-29070735-T-C
gnomAD v4: 2-29070735-T-C
MyVariant Identifiers: chr2:g.29293601T>C (hg19) chr2:g.29070735T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29070735T>C , CM000664.2:g.29070735T>C GRCh38
NC_000002.11:g.29293601T>C , CM000664.1:g.29293601T>C GRCh37
NC_000002.10:g.29147105T>C NCBI36
NG_021427.1:g.8527A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000331664.6:c.3527A>G MANE Select ENSP00000332809.4:p.Gln1176Arg
ENST00000331664.5:c.3527A>G ENSP00000332809.4:p.Gln1176Arg
NM_001029883.2:c.3527A>G NP_001025054.1:p.Gln1176Arg
XM_011532826.1:c.3527A>G XP_011531128.1:p.Gln1176Arg
XR_939901.1:n.185+1568T>C
XR_939902.1:n.173+1580T>C
NM_001029883.3:c.3527A>G MANE Select NP_001025054.1:p.Gln1176Arg
Search 100 bp 5'
Search 100 bp 3'