Canonical Allele Identifier: CA44640453

Gene: PCARE

Linked Data

• dbSNP Id: rs898677041
• MyVariant Identifiers: chr2:g.29294226C>T (hg19) ; chr2:g.29071360C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29071360C>T , CM000664.2:g.29071360C>T	GRCh38
NC_000002.11:g.29294226C>T , CM000664.1:g.29294226C>T	GRCh37
NC_000002.10:g.29147730C>T	NCBI36
NG_021427.1:g.7902G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331664.6:c.2902G>A MANE Select	ENSP00000332809.4:p.Gly968Arg
ENST00000331664.5:c.2902G>A	ENSP00000332809.4:p.Gly968Arg
NM_001029883.2:c.2902G>A	NP_001025054.1:p.Gly968Arg
XM_011532826.1:c.2902G>A	XP_011531128.1:p.Gly968Arg
XR_939901.1:n.185+2193C>T
XR_939902.1:n.173+2205C>T
NM_001029883.3:c.2902G>A MANE Select	NP_001025054.1:p.Gly968Arg