Canonical Allele Identifier: CA346472876
Gene: PCARE HGNC NCBI

Linked Data

dbSNP Id: rs1667458048
gnomAD v4: 2-29070688-T-C
MyVariant Identifiers: chr2:g.29293554T>C (hg19) chr2:g.29070688T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29070688T>C , CM000664.2:g.29070688T>C GRCh38
NC_000002.11:g.29293554T>C , CM000664.1:g.29293554T>C GRCh37
NC_000002.10:g.29147058T>C NCBI36
NG_021427.1:g.8574A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000331664.6:c.3574A>G MANE Select ENSP00000332809.4:p.Arg1192Gly
ENST00000331664.5:c.3574A>G ENSP00000332809.4:p.Arg1192Gly
NM_001029883.2:c.3574A>G NP_001025054.1:p.Arg1192Gly
XM_011532826.1:c.3574A>G XP_011531128.1:p.Arg1192Gly
XR_939901.1:n.185+1521T>C
XR_939902.1:n.173+1533T>C
NM_001029883.3:c.3574A>G MANE Select NP_001025054.1:p.Arg1192Gly
Search 100 bp 5'
Search 100 bp 3'