Canonical Allele Identifier: CA425617613
Gene: PCARE HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.29295957T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29073091T>G , CM000664.2:g.29073091T>G GRCh38
NC_000002.11:g.29295957T>G , CM000664.1:g.29295957T>G GRCh37
NC_000002.10:g.29149461T>G NCBI36
NG_021427.1:g.6171A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000331664.6:c.1171A>C MANE Select ENSP00000332809.4:p.Arg391=
ENST00000331664.5:c.1171A>C ENSP00000332809.4:p.Arg391=
NM_001029883.2:c.1171A>C NP_001025054.1:p.Arg391=
XM_011532826.1:c.1171A>C XP_011531128.1:p.Arg391=
XR_939901.1:n.185+3924T>G
XR_939902.1:n.173+3936T>G
NM_001029883.3:c.1171A>C MANE Select NP_001025054.1:p.Arg391=
Search 100 bp 5'
Search 100 bp 3'