Canonical Allele Identifier: CA346472805
Gene: PCARE HGNC NCBI

Linked Data

dbSNP Id: rs780134650

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29070650C>A , CM000664.2:g.29070650C>A GRCh38
NC_000002.11:g.29293516C>A , CM000664.1:g.29293516C>A GRCh37
NC_000002.10:g.29147020C>A NCBI36
NG_021427.1:g.8612G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000331664.6:c.3612G>T MANE Select ENSP00000332809.4:p.Gln1204His
ENST00000331664.5:c.3612G>T ENSP00000332809.4:p.Gln1204His
NM_001029883.2:c.3612G>T NP_001025054.1:p.Gln1204His
XM_011532826.1:c.3612G>T XP_011531128.1:p.Gln1204His
XR_939901.1:n.185+1483C>A
XR_939902.1:n.173+1495C>A
NM_001029883.3:c.3612G>T MANE Select NP_001025054.1:p.Gln1204His