Canonical Allele Identifier: CA346480286
Gene: PCARE HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.29295734A>C (hg19) chr2:g.29072868A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29072868A>C , CM000664.2:g.29072868A>C GRCh38
NC_000002.11:g.29295734A>C , CM000664.1:g.29295734A>C GRCh37
NC_000002.10:g.29149238A>C NCBI36
NG_021427.1:g.6394T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000331664.6:c.1394T>G MANE Select ENSP00000332809.4:p.Val465Gly
ENST00000331664.5:c.1394T>G ENSP00000332809.4:p.Val465Gly
NM_001029883.2:c.1394T>G NP_001025054.1:p.Val465Gly
XM_011532826.1:c.1394T>G XP_011531128.1:p.Val465Gly
XR_939901.1:n.185+3701A>C
XR_939902.1:n.173+3713A>C
NM_001029883.3:c.1394T>G MANE Select NP_001025054.1:p.Val465Gly
Search 100 bp 5'
Search 100 bp 3'