Canonical Allele Identifier: CA346480333
Gene: PCARE HGNC NCBI

Linked Data

ClinVar Variation Id: 1022149
ClinVar RCV Id: RCV001322020
dbSNP Id: rs1667517673
MyVariant Identifiers: chr2:g.29295758T>A (hg19) chr2:g.29072892T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29072892T>A , CM000664.2:g.29072892T>A GRCh38
NC_000002.11:g.29295758T>A , CM000664.1:g.29295758T>A GRCh37
NC_000002.10:g.29149262T>A NCBI36
NG_021427.1:g.6370A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000331664.6:c.1370A>T MANE Select ENSP00000332809.4:p.Asp457Val
ENST00000331664.5:c.1370A>T ENSP00000332809.4:p.Asp457Val
NM_001029883.2:c.1370A>T NP_001025054.1:p.Asp457Val
XM_011532826.1:c.1370A>T XP_011531128.1:p.Asp457Val
XR_939901.1:n.185+3725T>A
XR_939902.1:n.173+3737T>A
NM_001029883.3:c.1370A>T MANE Select NP_001025054.1:p.Asp457Val
Search 100 bp 5'
Search 100 bp 3'