Canonical Allele Identifier: CA425438028
Gene: PCARE HGNC NCBI

Linked Data

dbSNP Id: rs1413645061
gnomAD v2: 2-29293588-A-T
gnomAD v4: 2-29070722-A-T
MyVariant Identifiers: chr2:g.29293588A>T (hg19) chr2:g.29070722A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29070722A>T , CM000664.2:g.29070722A>T GRCh38
NC_000002.11:g.29293588A>T , CM000664.1:g.29293588A>T GRCh37
NC_000002.10:g.29147092A>T NCBI36
NG_021427.1:g.8540T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000331664.6:c.3540T>A MANE Select ENSP00000332809.4:p.Ala1180=
ENST00000331664.5:c.3540T>A ENSP00000332809.4:p.Ala1180=
NM_001029883.2:c.3540T>A NP_001025054.1:p.Ala1180=
XM_011532826.1:c.3540T>A XP_011531128.1:p.Ala1180=
XR_939901.1:n.185+1555A>T
XR_939902.1:n.173+1567A>T
NM_001029883.3:c.3540T>A MANE Select NP_001025054.1:p.Ala1180=
Search 100 bp 5'
Search 100 bp 3'