Canonical Allele Identifier: CA425616456
Gene: PCARE HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.29293702T>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29070836T>A , CM000664.2:g.29070836T>A GRCh38
NC_000002.11:g.29293702T>A , CM000664.1:g.29293702T>A GRCh37
NC_000002.10:g.29147206T>A NCBI36
NG_021427.1:g.8426A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000331664.6:c.3426A>T MANE Select ENSP00000332809.4:p.Pro1142=
ENST00000331664.5:c.3426A>T ENSP00000332809.4:p.Pro1142=
NM_001029883.2:c.3426A>T NP_001025054.1:p.Pro1142=
XM_011532826.1:c.3426A>T XP_011531128.1:p.Pro1142=
XR_939901.1:n.185+1669T>A
XR_939902.1:n.173+1681T>A
NM_001029883.3:c.3426A>T MANE Select NP_001025054.1:p.Pro1142=
Search 100 bp 5'
Search 100 bp 3'