Canonical Allele Identifier: CA346475943
Gene: PCARE HGNC NCBI

Linked Data

dbSNP Id: rs746136694

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29071234G>C , CM000664.2:g.29071234G>C GRCh38
NC_000002.11:g.29294100G>C , CM000664.1:g.29294100G>C GRCh37
NC_000002.10:g.29147604G>C NCBI36
NG_021427.1:g.8028C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000331664.6:c.3028C>G MANE Select ENSP00000332809.4:p.Arg1010Gly
ENST00000331664.5:c.3028C>G ENSP00000332809.4:p.Arg1010Gly
NM_001029883.2:c.3028C>G NP_001025054.1:p.Arg1010Gly
XM_011532826.1:c.3028C>G XP_011531128.1:p.Arg1010Gly
XR_939901.1:n.185+2067G>C
XR_939902.1:n.173+2079G>C
NM_001029883.3:c.3028C>G MANE Select NP_001025054.1:p.Arg1010Gly