Canonical Allele Identifier: CA346474922
Gene: PCARE HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.29293694G>T (hg19) chr2:g.29070828G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29070828G>T , CM000664.2:g.29070828G>T GRCh38
NC_000002.11:g.29293694G>T , CM000664.1:g.29293694G>T GRCh37
NC_000002.10:g.29147198G>T NCBI36
NG_021427.1:g.8434C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000331664.6:c.3434C>A MANE Select ENSP00000332809.4:p.Pro1145Gln
ENST00000331664.5:c.3434C>A ENSP00000332809.4:p.Pro1145Gln
NM_001029883.2:c.3434C>A NP_001025054.1:p.Pro1145Gln
XM_011532826.1:c.3434C>A XP_011531128.1:p.Pro1145Gln
XR_939901.1:n.185+1661G>T
XR_939902.1:n.173+1673G>T
NM_001029883.3:c.3434C>A MANE Select NP_001025054.1:p.Pro1145Gln
Search 100 bp 5'
Search 100 bp 3'