Canonical Allele Identifier: CA425616851
Gene: PCARE HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.29294050C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29071184C>T , CM000664.2:g.29071184C>T GRCh38
NC_000002.11:g.29294050C>T , CM000664.1:g.29294050C>T GRCh37
NC_000002.10:g.29147554C>T NCBI36
NG_021427.1:g.8078G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000331664.6:c.3078G>A MANE Select ENSP00000332809.4:p.Val1026=
ENST00000331664.5:c.3078G>A ENSP00000332809.4:p.Val1026=
NM_001029883.2:c.3078G>A NP_001025054.1:p.Val1026=
XM_011532826.1:c.3078G>A XP_011531128.1:p.Val1026=
XR_939901.1:n.185+2017C>T
XR_939902.1:n.173+2029C>T
NM_001029883.3:c.3078G>A MANE Select NP_001025054.1:p.Val1026=
Search 100 bp 5'
Search 100 bp 3'