Canonical Allele Identifier: CA425616726
Gene: PCARE HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.29294152T>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29071286T>C , CM000664.2:g.29071286T>C GRCh38
NC_000002.11:g.29294152T>C , CM000664.1:g.29294152T>C GRCh37
NC_000002.10:g.29147656T>C NCBI36
NG_021427.1:g.7976A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000331664.6:c.2976A>G MANE Select ENSP00000332809.4:p.Arg992=
ENST00000331664.5:c.2976A>G ENSP00000332809.4:p.Arg992=
NM_001029883.2:c.2976A>G NP_001025054.1:p.Arg992=
XM_011532826.1:c.2976A>G XP_011531128.1:p.Arg992=
XR_939901.1:n.185+2119T>C
XR_939902.1:n.173+2131T>C
NM_001029883.3:c.2976A>G MANE Select NP_001025054.1:p.Arg992=
Search 100 bp 5'
Search 100 bp 3'