Canonical Allele Identifier: CA425438025
Gene: PCARE HGNC NCBI

Linked Data

ClinVar Variation Id: 1651692
ClinVar RCV Id: RCV002155829
dbSNP Id: rs370727666
MyVariant Identifiers: chr2:g.29293587G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29070721G>A , CM000664.2:g.29070721G>A GRCh38
NC_000002.11:g.29293587G>A , CM000664.1:g.29293587G>A GRCh37
NC_000002.10:g.29147091G>A NCBI36
NG_021427.1:g.8541C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000331664.6:c.3541C>T MANE Select ENSP00000332809.4:p.Leu1181=
ENST00000331664.5:c.3541C>T ENSP00000332809.4:p.Leu1181=
NM_001029883.2:c.3541C>T NP_001025054.1:p.Leu1181=
XM_011532826.1:c.3541C>T XP_011531128.1:p.Leu1181=
XR_939901.1:n.185+1554G>A
XR_939902.1:n.173+1566G>A
NM_001029883.3:c.3541C>T MANE Select NP_001025054.1:p.Leu1181=
Search 100 bp 5'
Search 100 bp 3'